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  • Dispositivo 1211
  • Fabricante 31827
  • Evento 5885
  • Implante 4142
Device Recall NexGen Complete Knee Solution Monoblock Tibial Provisional/Drill Guide
  • Modelo / Serial
    Part number 00-5887-045-00 Lot number 62592928
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US Distribution and the countries of Australia and Denmark.
  • Descripción del producto
    NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill Guide Tibial Size 5 Femoral Size Green / CH || Zimmer U.K. Ltd., SN3 4FP, UK || Zimmer Trabecular Metal Technology, Inc || 10 Pomeroy Road, Parsippany, NJ 07054 USA
  • Manufacturer
    Zimmer Trabecular Metal Technology, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall NexGen Complete Knee Solution Monoblock Tibial Provisional/Drill Guide
Device Recall ORTHOSENSOR KNEE BALANCER, VERASENSE KNEE SYSTEM
  • Modelo / Serial
    Model SYK-TRCR 02, Lot # 091914V11770, Serial #s: 411654008, 411585023, 411654007, 411585032, 411585014, 411654016, 411585017, 411654015, 411585030, 411654020, 411654004, 411654010, 411585007, 411585005, 411654011, 411585036, 411585035, 411654018, 411654012, 411585011, 411654014, 411654005, 411654001, 411585003.
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Distribution to the states of : IL, MI, NY, CA, VA and NV.
  • Descripción del producto
    Verasense Knee System, Model SYK-TRCR 02. Intelligent disposable tibial insert that measures dynamic loads during orthopedic knee surgery.
  • Manufacturer
    Orthosensor, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall ORTHOSENSOR KNEE BALANCER, VERASENSE KNEE SYSTEM
Device Recall ATTUNE INTUITION
  • Modelo / Serial
    CATALOG NO. : 2544-01-017 LOT NUMBER: All Lots Barcode GTIN: 10603295423324
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-US (nationwide) except AK and RI, including PR and the countries of Chile, Canada, Australia, Austria, Belgium, France, Hong Kong, Ireland, India, Israel, Italy, Japan, Malaysia, Netherlands, New Zealand, Saudi Arabia, Singapore, Slovakia, South Africa, South Korea, Spain, Switzerland, Thailand, United Arab Emirates (UAE), and United Kingdom (UK
  • Descripción del producto
    The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized in knee replacement procedures. The instrument interfaces with several related ATTUNE instruments: keel punch, tibial tower, evaluation bullet, fixed bearing tibial impactor, rotating platform tibial impactor, and femoral impactor, for the purpose of impaction, extraction, and insertion applications at steps within the surgical procedure. Due to the frequency of its use, two impaction handles are supplied in each kit.
  • Manufacturer
    DePuy Orthopaedics, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall ATTUNE INTUITION
Device Recall Mandible Locking Plate (MLP) Bender / Cutter
  • Modelo / Serial
    Sold Lot Numbers: 4520830 4519339 4528112 4527510 4527509 4528678 4529517 4532428 4542201 4547106 4547107 4548231 4552202 4552203 4562899 4566835 4572774 4572775 4578754 4581035 4593516 4738938 4768238 4805320 4805321 4805622 4805623 4814351 4869678 4871808 4880493 4880495 4888588 4915212 4915213 4935249 4935250 4964319 4964324 4973229 5021231 5021232 5021233 5036650 5036651 5056855 5056154 5056856 5079563 5079564 5079565 5079538 5090675 5090677 5105352 5144695 5144697 5144696 5161969 5161970 5191074 5196260 5229584 5229586 5229585 5229587 5253009 5256476 5256477 5262049 5267000 5276395 5278583 5283776 5283780 5353853 5360628 5367534 5367535 5370545 5388335 5370546 5388336 5765950 5775823; Manufacturing Lot Number A7LA49 A7LA48 A7LA51 A7LA50 A7LA50 A7LA51 A7LA51 A7LA47 A7MA03 A7MA05 A7MA05 A7MA05 A7MA06 A7MA06 A7MA09 A7MA10 A7MA11 A7MA11 A7MA13 A7MA14 A7MA18 A7NA08 A7NA08 A7NA25 A7NA25 A7NA25 A7NA25 A7NA25 A7NA40 A7NA41 A7NA43 A7NA43 A7NA43 A7NA43 A7NA51 A7NA52 A7NA51 A7OA09 A7OA09 A7OA09 A7OA21 A7OA21 A7OA21 A7OA24 A7OA24 A7OA30 A7OA29 A7OA33 A7OA29 A7OA35 A7OA35 A7OA36 A7OA38 A7OA38 A7OA41 A7OA50 A7OA50 A7OA50 A7OA51 A7OA51 A7PA07 A7PA08 A7OA50 A7OA51 A7PA08 A7PA07 A7PA20 A7PA21 A7PA21 A7PA21 A7PA23 A7PA23 A7PA24 A7PA25 A7PA25 A7PA39 A7PA40 A7PA41 A7PA41 A7PA42 A7PA41 A7PA42 A7PA43 A7PA47 A7PA47
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- US and Canada.
  • Descripción del producto
    2.0 Mandible Locking Plate (MLP) Bender / Cutter (part number 329.143) || Intended to be used for bending and/or cutting Mandible Locking Plates.
  • Manufacturer
    Synthes, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Mandible Locking Plate (MLP) Bender / Cutter
Device Recall POWEREASE(TM) Instruments Set Screw Breakoff Instrument
  • Modelo / Serial
    Lot # - CA14C107
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    US Distribution to the states of : CA, KS, KY, NC, TX, WA, MI, OH, IA, PA, OR, MS, FL, NY, GA and AR.
  • Descripción del producto
    POWEREASE Instruments Set Screw Breakoff Instrument, REF 2346010, Medtronic Sofamor Danek, USA, Inc. Spinal surgical instrumrent.
  • Manufacturer
    Medtronic Sofamor Danek USA Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall POWEREASE(TM) Instruments Set Screw Breakoff Instrument
Device Recall Fixed Tibial bearing ATTUNE INTUITION Impactor
  • Modelo / Serial
    CATALOG NO. : ATTUNE INTUITION Impactors  Fixed Tibial Bearing, (254401003)  Barcode GTIN Number:  Fixed Tibial Bearing, ......... 10603295130192   ALL LOTS
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution: US (nationwide) including P.R. except AK and RI; and Internationally to: Chile, Canada, Australia, Austria, Belgium, China, France, Ireland, India, Israel, Italy, Japan, Malaysia, Netherlands, New Zealand, Singapore, Slovakia, South Africa, South Korea, Spain, Switzerland, Thailand, United Arab Emirates (UAE), and United Kingdom (UK).
  • Descripción del producto
    Fixed Tibial bearing ATTUNE INTUITION Impactor || The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home its relevant mating part: Fixed Tibial bearing, (254401003) Rotating Tibial Platform, (254401004) and Femoral impactor, (254401006).
  • Manufacturer
    DePuy Orthopaedics, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Fixed Tibial bearing ATTUNE INTUITION Impactor
Device Recall Rotating Tibial Platform ATTUNE INTUITION Impactor
  • Modelo / Serial
    CATALOG NO. : ATTUNE INTUITION Impactors  Rotating Tibial Platform, (254401004)  Barcode GTIN Number:  Rotating Tibial Platform, ......... 10603295130208  ALL LOTS
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution: US (nationwide) including P.R. except AK and RI; and Internationally to: Chile, Canada, Australia, Austria, Belgium, China, France, Ireland, India, Israel, Italy, Japan, Malaysia, Netherlands, New Zealand, Singapore, Slovakia, South Africa, South Korea, Spain, Switzerland, Thailand, United Arab Emirates (UAE), and United Kingdom (UK).
  • Descripción del producto
    Rotating Tibial Platform ATTUNE INTUITION Impactor. || The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home its relevant mating part: Fixed Tibial bearing, (254401003) Rotating Tibial Platform, (254401004) and Femoral impactor, (254401006).
  • Manufacturer
    DePuy Orthopaedics, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Rotating Tibial Platform ATTUNE INTUITION Impactor
Device Recall Femoral Impactor ATTUNE INTUITION Impactor
  • Modelo / Serial
    CATALOG NO. : ATTUNE INTUITION Impactors  Femoral Impactor, (254401006)  Barcode GTIN Number:  Femoral Impactor, 10603295130222  ALL LOTS
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution: US (nationwide) including P.R. except AK and RI; and Internationally to: Chile, Canada, Australia, Austria, Belgium, China, France, Ireland, India, Israel, Italy, Japan, Malaysia, Netherlands, New Zealand, Singapore, Slovakia, South Africa, South Korea, Spain, Switzerland, Thailand, United Arab Emirates (UAE), and United Kingdom (UK).
  • Descripción del producto
    Femoral Impactor ATTUNE INTUITION Impactor. || The ATTUNE INTUITION Impactors are re-useable instruments utilized in knee replacement procedures. The three affected impactors are used at various times within the surgical flow, each impactor is used to impact and drive home its relevant mating part: Fixed Tibial bearing, (254401003) Rotating Tibial Platform, (254401004) and Femoral impactor, (254401006).
  • Manufacturer
    DePuy Orthopaedics, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Femoral Impactor ATTUNE INTUITION Impactor
Device Recall HP LCS IM Hole Locator instrument
  • Modelo / Serial
    CATALOG NO. : 9505-01-041 Barcode GTIN: 10603295224389 ALL LOTS
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution: US (nationwide) including states of: AZ, CA, CO, FL, GA, HI, IA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MT, NC, NV, NY, OH, PA, TN, TX, VA, WA, and WI; and countries of: Canada, Australia, Austria, Belgium, Czech Republic, France, Germany, India, Israel, Italy, Japan, Malaysia, Russia, South Africa, Switzerland, and United Kingdom.
  • Descripción del producto
    I.M. Hole Locator Instrument. Orthopedic manual surgical instrument. || The IM Hole locator guides the IM drill during IM Hole preparation. The instrument is positioned between the condyles and aligned with the anatomical axis. Pins can be placed in the IM hole locator to assist with additional stability. The drill bush may also be lightly impacted onto the distal femur for additional stability.
  • Manufacturer
    DePuy Orthopaedics, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall HP LCS IM Hole Locator instrument
Device Recall SpineFrontier PedFuse Pedicle Screw System
  • Modelo / Serial
    Lot/Serial Numbers: 06440-0000, 06441-0000, AG24
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including TX, OH, VA, and Washington, DC.
  • Descripción del producto
    lnline Persuader- PedFuse Pedicle Screw System; Part Number: 11-80164
  • Manufacturer
    SpineFrontier, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall SpineFrontier PedFuse Pedicle Screw System
Device Recall Synthes Electric Pen Drive (EPD) System
  • Modelo / Serial
    Part Number  05.001.012  Lot Numbers AV18166 AV19044 AV20666
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Synthes Electric Pen Drive (EPD) System, The Synthes Electric Pen Drive is indicated for screw insertion, pin and wire replacement, cutting of bone and metal, drilling, decorticating, shaping, and smoothing of bones and teeth in a wide variety of surgical procedures, including, but not limited to general orthopaedic trauma, foot, hand, maxillofacial, neurosurgical, oral, otolaryngolical, reconstructive, and spine surgery.
  • Manufacturer
    Synthes, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Synthes Electric Pen Drive (EPD) System
Device Recall Brainlab AG
  • Modelo / Serial
    Model 52856 BL CURVED CUP INSERTER UNIVERSAL SHAFT; and MODEL 52856A BL OFFSET CUP IMPACTOR UNIVERSAL SHAFT, all serial/lot numbers distributed prior to January 13, 2015.
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US: Nationwide (AZ, CA, ID, IL, MD, MI, MN, OH, OK, OR, TN, WA, WI, WV); Australia, Austria, Bahrain, Belgium, Germany, Hong Kong, India, Italy, Japan, Malaysia, Russian Federation, Saudi Arabia, South Korea, Spain, Switzerland, Thailand, United Arab Emirates, United Kingdom
  • Descripción del producto
    The Brainlab Offset Cup Impactor Universal. Part of the Brainlab hip system. An intraoperative image-guided localization system to enable minimally invasive orthopedic surgery. (a stereotaxic instrument)
  • Manufacturer
    Brainlab AG
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Brainlab AG
Device Recall System 6 Aseptic Housing
  • Modelo / Serial
    Part No. 6126-120-000, Lots 13205, 13209, 13210, 13212
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-US (nationwide) including Puerto Rico and the states of AR, CA, CO, FL, GA, HI, MD, NC, NY, PA, SC, TX, and VA, and the countries of Australia, Canada, Switzerland, Hong Kong, South Africa, Chile, Korea, Poland, India, Colombia, The Netherlands, and France.
  • Descripción del producto
    System 6 Aseptic Housing. || The Stryker System 6 Aseptic Housings provide a sterile enclosure for the Stryker Non-sterile Battery. Accessory for powered orthopedic surgical instrument.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall System 6 Aseptic Housing
Device Recall Robotic Arm Interactive Orthopedic System (RIO)
  • Modelo / Serial
    All lots, Part Numbers: 201000, 203999, 207300, and 209930.
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution-including the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, LA, MA, MD, MI, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV and Hawaii.
  • Descripción del producto
    Restoris Partial Knee Application (PKA) RIO (TGS 2.0). || For use with the Robotic Arm Interactive Orthopedic System (RIO), is indicated for use in surgical knee procedures.
  • Manufacturer
    Mako Surgical Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Robotic Arm Interactive Orthopedic System (RIO)
Device Recall KYPHON(R) EXPRESS(TM), Osteo Introducer(R) System, Diamond and Bevel, Size 2
  • Modelo / Serial
    WI14H054
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide and Canada
  • Descripción del producto
    KYPHON EXPRESS, Osteo Introducer System, Diamond and Bevel, Size 2, REF T34A, QTY: 1EA, Rx only, STERILE R. For use with spinal fixation devices.
  • Manufacturer
    Medtronic Sofamor Danek USA Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall KYPHON(R) EXPRESS(TM), Osteo Introducer(R) System, Diamond and Bevel, Size 2
Device Recall Synthes Inserter for Titanium Elastic Nails
  • Modelo / Serial
    Part Number: 359.219,  Sold As Lot Numbers: 4321659 4340451 4466686 4470900 5496455 5700078 5718485 5718486 5718487 1904339 3005674 3005675 3009312 3020674 3025607 3051190 3054608 3065013 3069566 3084637 3098634 3121438 3232931 3242304 3262712 3301017 3325276 3382583 3410330 3430483 3493588 3504996 3524633 3619119 3626055 3659645 3706611 3797835 7505411 7565990 7601112 7619995 7670741 7675623 7727696 7774491 7810649 7845943 7874224 7896075 7979727 4796463 4826021 4911859 4911860 4969014 4971314 5066417 5042001 5066418 5090226 5090224 5106335 5123586 5162204 5123587 5162205 5162206 5162760 5181760 5181761 5227459 5236654 5258103 5420946 5422955 5455364 5455365 5507788 5525235 5485078 5492810 5545372 5555604 5569028 5611445 5611446 5611447 5641430 5670475 5641429 5657075 5657073 5670474 5700077 5700079 8114862 8214803 8326267 8424513 8476286 8541845 8608192 8608193 8768253 8973607 9275702 4389269 4537554 4594280 4594281 4825384;  (Manufacturing Lot Numbers: 1095607 1095607 1121876 1121876 1641700 1806500 1811056 1811059 1813900 1904339 3005674 3005675 3009312 3020674 3025607 3051190 3054608 3065013 3069566 3084637 3098634 3121438 3232931 3242304 3262712 3301017 3325276 3382583 3410330 3430483 3493588 3504996 3524633 3619119 3626055 3659645 3706611 3797835 7505411 7565990 7601112 7619995 7670741 7675623 7727696 7774491 7810649 7845943 7874224 7896075 7979727 8000136 8002518 8002635 8002635 8004538 8004538 8005179 8006103 8006214 8006214 8006578 8006578 8007139 8007139 8007472 8007472 8008046 8008046 8008046 8008261 8009205 8009363 8009859 8012109 8012353 8012925 8013244 8014078 8014078 8014645 8014645 8015605 8015831 8016063 8016128 8016128 8016128 8016423 8016423 8016759 8017447 8017590 8017862 8017872 8018319 8114862 8214803 8326267 8424513 8476286 8541845 8608192 8608193 8768253 8973607 9275702 A8LA901 A8MA648 A8MB744 A8NA025 A8NA430)
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Synthes Inserter for Titanium Elastic Nails; The Inserter for Titanium Elastic Nails (TEN) is intended for fixation of diaphyseal fractures where the canal is narrow or flexibility of the implant is paramount. This includes: lower extremity fractures in pediatric and small-statured patients and upper extremity fractures in patients. || This system is also intended to treat metaphyseal and episphyseal fractures, such as radial neck fractures, and is intended for fixation of small long bones, such as carpal and tarsal bones. In pediatric applications, the flexibility of the elastic nail allows it to be inserted at a point which avoids disruption of the bone growth plate.
  • Manufacturer
    Synthes, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Synthes Inserter for Titanium Elastic Nails
Device Recall RECLAIM Revision Hip System; Assembled Implant Inserter Adaptor
  • Modelo / Serial
    CATALOG NO. : 2975-00-920:  Barcode (GTIN): 10603295156192 Lot No. Distribution SO2018074 (Distributed) SO2018072 (Not Distributed) SO2018073 (Not Distributed) SO2018075 (Not Distributed) SO2018080 (Not Distributed)
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution: US (nationwide) in CA; Ireland and Israel.
  • Descripción del producto
    RECLAIM Assembled Implant Inserter Adaptor orthopedic manual surgical instrument for hip implantation.
  • Manufacturer
    DePuy Orthopaedics, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall RECLAIM Revision Hip System; Assembled Implant Inserter Adaptor
Device Recall Reamers Orthopedic manual surgical instrument
  • Modelo / Serial
    Part #: PI-0507, Lot #s:1308811A, 1457704A; Part #: PI-0508, Lot #s: 1308812A, 1457705A; Part #: PI-0509, Lot #s: 1038813A, 1457706A; Part #: PI-0510, Lot #s: 1308814A, 1457707A; Part #: PI-0511, Lot #s: 1308815A, 1457708A; Part #: PI-0512, Lot #s: 1308816A, 1457709A; Part #: PI-0513, Lot #s: 1308817A, 1457710A; Part #: PI-0514, Lot #s: 1308818A, 1457711A; Part #: PI-0507-S, Lot #: 2130005; Part #: PI-0508-S, Lot #: 2130006; Part #: PI-0509-S, Lot #: 2130007; Part #: PI-0510-S, Lot #: 2130008; Part #: PI-0511-S, Lot #: 2130009; Part #: PI-0512-S, Lot #: 2130010; Part #: PI-0513-S, Lot #:2130011; Part #: PI-0514-S, Lot #: 2130012
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    GA, IN, FL, UT, AZ, CA, and NY
  • Descripción del producto
    Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers).
  • Manufacturer
    Captiva Spine, Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Reamers Orthopedic manual surgical instrument
Device Recall Instrument Kit for use with OsteoSponge SC grafts
  • Modelo / Serial
    SERIAL NUMBERS:  004, 005, 006, 009, 010, 011, 012, 018, 019, 020, 021, 022, 023, 024, 025, 026, 029, 30, 033, 036, 038, 040, 045, 048, 060, 063, 064, 065, 066, 067, 068, 069, 070, 071, 072, 073, 074, 075, 076, 077, 079, 081, 082, 083, 084, 085, 086, 087, 088, 089, 090, 091, 092, 093, 094, 095, 096, 097, 098, 099, 100, 101, and 102.
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    US Distribution in states of: Alabama, Arizona, Arkansas, Colorado, Florida, Georgia, Illinois, Indiana, Louisiana, Maryland, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Puerto Rico, Texas, and Virginia.
  • Descripción del producto
    Instrument Kit for use with OsteoSponge SC grafts. The Instrument Kit is used to insert OsteoSponge SC grafts to fill bone defects in the subchondral region of articulating joints. || The Instrument Kit is used to establish and maintain a port of entry for arthroscopic instruments or for an open procedure. The kit is also used to insert the OsteoSponge¿ SC graft during surgery. Such procedures include, but are not limited to, subchondral bone repair. || Affected Part numbers are 6508 and 6511.
  • Manufacturer
    Bacterin International, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Instrument Kit for use with OsteoSponge SC grafts
Device Recall Lineum HF Torque Handle Limit (Lineum)
  • Modelo / Serial
    538133 ,538134 ,548080 ,550475 ,552169 ,553131, 553710 ,558873 ,567568 ,569141
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US Nationwide
  • Descripción del producto
    Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 || P_roduct Usage: || Designed to facilitate reconstruction of the cervical and upper thoracic spine using bones screws, locking plugs, and various types of rods, hooks, and lateral connectors.
  • Manufacturer
    Biomet Spine, LLC
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Lineum HF Torque Handle Limit (Lineum)
Device Recall Torque Limiting Handle (Aspen/ Alpine)
  • Modelo / Serial
    538133,538134,548080,550475,552169,553131,553710,558873,567568,569141  Part Number: 6200-1109 2009300344 to 2009300543  2009300544 to 2009300643  2009300644 to 2009300743  2009300744 to 2009300843  2009300844 to 2009300993  2009411328 to 2009411377  2010082160 to 2010082257  2010152507 to 2010152571  2010373025 to 2010373174
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US Nationwide
  • Descripción del producto
    Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 || Product Usage: || Provides posterior fixation in the non-cervical spine with an interspinous fixation device.
  • Manufacturer
    Biomet Spine, LLC
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Torque Limiting Handle (Aspen/ Alpine)
Device Recall Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021
  • Modelo / Serial
    ALL Lots
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (nationwide including DC, Hawaii, and Puerto Rico) and Internationally to Argentina, Austria, Australia, Belgium, Bahrain, Bolivia, Brazil, Canada, China, Chile, Costa Rica, Czech Republic, Germany, Denmark, Ecuador, Egypt, Spain, Finland, France, Great Britain, Greece, Guatemala, Hong Kong, Croatia, Hungary, Indonesia, Ireland, Israel, India, Iraq, Iran, Italy, Jordan, Japan, Kenya, Korea, Kuwait, Lebanon, Sri Lanka, Libyan Arab Jamahiriya, Morocco, Macedonia, Mexico, Malaysia, Netherlands, Norway, Nepal, New Zealand, Oman, Ontario, Peru, Philippines, Palestine, Portugal, Romania, Serbia, Russian Federation, Saudi Arabia, Sweden, Singapore, Slovenia, Slovakia, South Africa, El Salvador, Thailand, Turkey, Taiwan, Ukraine, Uruguay, Venezuela, Vietnam and United Arab Emirates.
  • Descripción del producto
    Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 for orthopedic surgery.
  • Manufacturer
    The Anspach Effort, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021
Device Recall Stryker Instruments
  • Modelo / Serial
    Part No. 7110-120-000; Affected serial numbers as follows: 1234701323, 1402902743, 1402902893, 1221503173, 326305393, 1217705113, 1315004963, 1222700863, 1326305403, 1217705123, 1315005013, 1222701093, 1217705283, 1324801023, 1217705083, 1322600723, 1217900123, 1324801083, 1217705093, 1305900203, 1210305253, 1407105433, 1217705133, 1306611063, 1400202023, 1409403273, 1334302313, 1307105733, 1400202103, 1205304123, 1334302333, 1307801973, 1402104293, 1205304133, 1334302363, 1307801983, 1402205583, 1207500553, 1334302413, 1307801993, 1301614823, 1426000013, 1334302433, 1207500593, 1301700663, 1326902543, 1305903843, 1207500603, 1326902613, 1326902563, 1333709623, 1302910113, 1327000033, 1327000253, 1333709633, 1302910133, 1327000073, 1232007733, 1333904723, 1305601713, 1317000743, 1317801313, 1333904773, 1305601723, 1302904613, 1317801323, 1333904813, 1305601733, 1303706253, 1214307613, 1333904873, 1323407973, 1314100963, 1214307753, 1317801293, 1323408113,  1314101093, 1214307763, 1325205193, 1323400563, 1235214993, 1317601493, 1325205203, 1323400553,  1235301413, 1317601503, 1326202573, 1323408133, 1210703413, 1317601513, 1326202643, 1323400503, 1326902663, 1317601573, 1326202853, 1406900423, 1229005743, 1317601613, 1221503193, 1131901973,  1301801283, 1317601633, 1221503243, 1132100013, 1317819563, 1317601693, 1204005873, 1210703303, 1329401733, 1319703043, 1205304433, 1210703333,  1400205393, 1314908463, 1217900203, 1302904713,  1401603423, 1314908763, 1221503143 & 1303706283      1317000303 1403013923 1327200633 1314100863 1317000523 1407601743 1221503113 1214307743 1207500493 1407601793 1222700883 1130600583 1207500523 1418913743 1222700973 1206101153 1207500533 1418913753 1222701063 1316303583 1207500543 1210703193 1317819693 1316303623 1227519993 1403013973 1327000133 1316303633 1300700303 1403013983 1327000143 1316303683 1300700313 1403013993 1307801883 1331806133 1300700323 1403014013 1210703133 1317000103 1327000283 1407612643 1214307963 1424507203 1327000293 1407704073 1410600103 1235301433 1327200503 1323300233 1410600153 1323300043 1327200513 1327200793 1411403473  1131902043 1328301563 1314908553  1132104893 1405701193 1315004953  1132104913 1407105423 1400802183  1426708823 1422701313 1400802193  1426708913 1200517413 1403605973  1413202093 1220102783 1403605993  1229300363 1221503073 1307802023  1230306343 1331708343 1419014663  1230306503 1331708413 1434400853  1234701653 1409000143 1434401073  1501309733 1409000183 1434401083  1217705053 1326305483 1413301453  1217705063 1326902363 1227520063  1305900263 1326902373 1312903303  1225601423 1326902383 1312906633  1414202943 1327200613 1314100813
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    US Nationwide in the states of AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MD, MI, MO, MS, MT, NC, NH, NV, NY, OH, OK, PA, SC, TN, TX, UT, VA, VT, WA, WI and the foreign country of: Canada
  • Descripción del producto
    Universal Charger || Product Usage: The Stryker Universal Battery Charger is designed to be used in conjunction with and provide power to non-sterile and sterile batteries. The Stryker Universal Battery Charger is a four station, modular battery charger intended to charge Stryker handpiece battery packs only. The battery charger has the optional functionality to track device usage data. Usage data is accumulated by Stryker and reports are able to be provided to the customer. || For powered surgical instruments.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Stryker Instruments
Device Recall Zimmer Anatomical Shoulder Handle for Rasp
  • Modelo / Serial
    Lot Number(s):  13870129 &  13878179.
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Distributed to the states of IN, GA, WI, MO, PA, KS, TN, and NY.
  • Descripción del producto
    Anatomical Shoulder Handle for Rasp || Item: 01.04233.000 || Used during total joint arthroplasty of the shoulder.
  • Manufacturer
    Zimmer Gmbh
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Zimmer Anatomical Shoulder Handle for Rasp
Device Recall Cannulated Drill Bits
  • Modelo / Serial
    Part Number  310.65 310.67 310.221  lot numbers  PE00966  PE01000 PE01039 PE01058 PE00959  PE00968 PE00974 PE00998 PE01006 PE01011 PE01048 PE00971  PE01059 PE01040
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (nationwide) and Canada.
  • Descripción del producto
    3.2 mm Cannulated Drill Bit/ QC 170 mm || 2.7 Cannulated Drill Bit/ QC 160 mm || 2.0 mm Cannulated Drill Bit / QC 150 mm || there is no indication for Synthes Cannulated Drill Bits which is used with the Synthes Cannulated Screw. The Synthes Cannulated Screw, used with the threaded washer, is generally intended for intra-articular fixation of small bones, such as the hand, wrist, and forefoot.
  • Manufacturer
    Synthes, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Cannulated Drill Bits
  • 1
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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.