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  • Dispositivo 26490
  • Fabricante 33665
  • Evento 35826
  • Implante 7175
Device Recall Raymond Corporation ForkTip Laser Guide
  • Modelo / Serial
    Model #1096597/001
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Raymond Laser alignment guide - Model #1096597/001 Green Laser. || Intended to assist operators in performing material handling activities such as storing and retrieving pallets and material in and on racking projecting a line onto a pallet or other material storage medium for assisting the operator in determining the position of the powered industrial truck forks with respect to load.
  • Manufacturer
    The Raymond Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Raymond Corporation ForkTip Laser Guide
Device Recall Raymond Corporation ForkTip Laser Guide
  • Modelo / Serial
    Model #1096597/002
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Raymond Laser alignment guide - Model #1096597/002 Red Laser. || Intended to assist operators in performing material handling activities such as storing and retrieving pallets and material in and on racking projecting a line onto a pallet or other material storage medium for assisting the operator in determining the position of the powered industrial truck forks with respect to load.
  • Manufacturer
    The Raymond Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Raymond Corporation ForkTip Laser Guide
Device Recall Hamamatsu Microfocus Xray Source
  • Modelo / Serial
    Series L8601, L9121, L7901, and L8031
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-- USA (nationwide) and the country of Canada.
  • Descripción del producto
    Hamamatsu Corporation, Bridgewater NJ 08807 || Microfocus X-ray Source || L8601 series, L9121 series (90kV type MICROFOCUS X-RAY SOURCE), || L7901 series, and L8031 series (100kV type MICROFOCUS || x-ray source
  • Manufacturer
    Hamamatsu Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Hamamatsu Microfocus Xray Source
Device Recall Laserworld
  • Modelo / Serial
    All projectors distributed between 2008 and 2012, including, but not limited to, the Proline Series AG, Revolution Series AG, Club Series AG, Clus Series, Pure Light Series, and Revolution Series AG
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    US Distribution including the states of CA, CO, FL, KS and PA.
  • Descripción del producto
    Laserworld RGB & Piko Nano RGB Models || All models are laser light show projectors, and will be used as such.
  • Manufacturer
    Laserworld Usa Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Laserworld
Device Recall Juno
  • Modelo / Serial
    Serial Numbers: 10110770 11030805 11070848 11070845 11070849 11030806 11090864 11110900 12020982 114087 12030999 12061020 12041003 12061014 12061018 12081040  :
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution including the states of AL, CA, CO, CT, IL, MD, MI, MO, NY, OH, PA
  • Descripción del producto
    Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose || Model: 70920 || Product Usage: || Universal R/F, general use
  • Manufacturer
    Philips Healthcare Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Juno
Device Recall Lockheed Martin Gyrocam Systems ( LMGS
  • Modelo / Serial
    Gyrocam DNV Camera System, Serial Numbers: 137, 138, 141, 142, 143, 144, 145, 148, 150, 151, 152, 158, 159, 160, 164, 165, 170, 172, 173, 174, 175, 177; Gyrocam DS Camera System, Serial Numbers: 134, 140, 147, 153, 169, 181; Gyrocam TS Camera System, Serial Numbers: 132, 146, 149, 171, 502.
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems. Laser pointer and illuminator used for law enforcement surveillance from aircraft. Models DNV, TS and DS
  • Manufacturer
    Lockheed Martin Gyrocam Systems, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Lockheed Martin Gyrocam Systems ( LMGS
Device Recall LHB, Type I First Aid Kit
  • Modelo / Serial
    All kits shipped between 1/12010 through 3/4/2013.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.
  • Descripción del producto
    LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg, Aspirin 4/pg and Povidone Iodine, antiseptic towelette. Kit Number: 2113110. || First Aid Kit.
  • Manufacturer
    Lighthouse For The Blind
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall LHB, Type I First Aid Kit
Device Recall LHB, Antiseptic Kit
  • Modelo / Serial
    All kits shipped between 1/12010 through 3/4/2013.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.
  • Descripción del producto
    LHB, Antiseptic Kit, Povidone Swab, Gauze Pads, and non-stick pads. Kit Number: 2113305. || First Aid Kit.
  • Manufacturer
    Lighthouse For The Blind
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall LHB, Antiseptic Kit
Device Recall LHB, First Aid Type I
  • Modelo / Serial
    All kits shipped between 1/12010 through 3/4/2013.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.
  • Descripción del producto
    LHB, First Aid Type I Individual Kit, NSN: 6545-00-656-1092, antiseptics, Kit number: 2114002. || First Aid Kit.
  • Manufacturer
    Lighthouse For The Blind
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall LHB, First Aid Type I
Device Recall LHB, Perishable Items Pack Type I
  • Modelo / Serial
    All kits shipped between 1/12010 through 3/4/2013.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.
  • Descripción del producto
    LHB, Perishable Items Pack Type I , Kit Number: 2114002-100. || First Aid Kit.
  • Manufacturer
    Lighthouse For The Blind
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall LHB, Perishable Items Pack Type I
Device Recall LHB, First Aid Type III
  • Modelo / Serial
    All kits shipped between 1/12010 through 3/4/2013.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.
  • Descripción del producto
    LHB, First Aid Type III, NSN # 6545-00-656-1094, Kit number: 2114011. || First Aid Kit.
  • Manufacturer
    Lighthouse For The Blind
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall LHB, First Aid Type III
Device Recall LHB, Perishable Item Pack Type III
  • Modelo / Serial
    All kits shipped between 1/12010 through 3/4/2013.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.
  • Descripción del producto
    LHB, Perishable Item Pack Type III. Kit number: 2114011-100. || First Aid Kit.
  • Manufacturer
    Lighthouse For The Blind
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall LHB, Perishable Item Pack Type III
Device Recall LHB, First Aid Type IV Belt Type
  • Modelo / Serial
    All kits shipped between 1/12010 through 3/4/2013.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.
  • Descripción del producto
    LHB, First Aid Type IV Belt Type, NSN #6545-01-010-7754. || Kit number: 114016. || First Aid Kit.
  • Manufacturer
    Lighthouse For The Blind
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall LHB, First Aid Type IV Belt Type
Device Recall LHB, Perishable Items Pack Type IV
  • Modelo / Serial
    All kits shipped between 1/12010 through 3/4/2013.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including DC and the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, MI, MD, MN, MO, MT, NC, NJ, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA and WY.
  • Descripción del producto
    LHB, Perishable Items Pack Type IV. Kit number: 2114016-100. || First Aid Kit.
  • Manufacturer
    Lighthouse For The Blind
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall LHB, Perishable Items Pack Type IV
Device Recall ORTHO Assay Software (OAS) Server
  • Modelo / Serial
    Serial numbers: 0811F06216 through 0811F06225 and 0911F06240 through 0911F06245 and 1011F06317 through 1011F06331
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA Nationwide including the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WI & WV, and countries of: Australia, Brazil, Canada, Chile, China, Colombia, India, Japan, Mexico, PR, Panama, Singapore, Venezuela, England, France, Germany, Italy, Spain
  • Descripción del producto
    ORTHO¿ Assay Software (OAS) Server, Catalog # 6842840 || Usage: || The ORTHO¿ Summit System (OSS) is a modular, integrated system for use with licensed blood screening tests. Consisting of networked processors and instruments linked together via a local area network, assay-specific pipetting protocols and ORTHO Assay Software (OAS), OSS automates many of the processing functions and data management requirements associated with ELISA (enzyme-linked immunosorbent assay) microplate testing.
  • Manufacturer
    Ortho-Clinical Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall ORTHO Assay Software (OAS) Server
Device Recall Digital Pathology System (DPS) Software, version 1.1
  • Modelo / Serial
    catalog # OMN-1005056-1, K1600LH, DPS 1.1
  • Clasificación del producto
    Hematology and Pathology Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    International Distribution to Canada and Switzerland only.
  • Descripción del producto
    Digital Pathology System (DPS) Software version 1.1 || The Omnyx" Integrated Digital Pathology system, which consists of a whole slide scanner and associated software applications, is a scanning, receiving, storing, managing, annotating and computer monitor viewing system for digital whole slide images. Omnyx" products are for in vitro diagnostic use for specific clinical applications, and are intended for research use only on other applications. Specific clinical use applications are indicated in separate clinical specific user guides supplied by Omnyx.
  • Manufacturer
    Omnyx Llc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Digital Pathology System (DPS) Software, version 1.1
Device Recall Distributed under various trade names
  • Modelo / Serial
    Lot Numbers are for kits and cabinets: C0207, C0217, C0227, C0267, C0277, C0287, C0297, C0307, D0027, D0037, D0047, D0057, D0067, D0097, D0107, D0117, D0127, D0137, D0167, D0177, D0187, D0197, D0207, D0247, D0267, E0027, E0047, E0077, E0087, E0177, E0187, D0227, E0297, E0307, E0317, F0017, F0087, F0207, F0267, G0067, G0097, G0137, G0187, G0257, H0017, H0157, H0167, H0237, H0277, H0287, H0297, H0307, H0317, I0047, I0057, I0107, I0127, I0137, I0177, I0187, I0197, I0207, I0217, I0247, I0251, I0277, I0287, J0017, J0037, J0047, J0087, J0097, and J0117.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Worldwide: USA and to one distributor in Dubai, United Arab Emirates.
  • Descripción del producto
    First Aid Kits, soft canvas, plastic, and metal containers holding various products to include ibuprofen and other first aid supplies, in various sizes. Kits include: || Labeled with First Aid Only, Inc. Vancouver, WA: || Recreational Sports First Aid, Item SM-134; || Welder's First Aid Kit, Item 253-U; || Vehicle First Aid Kit, Item 220-0; || On-The-Road Auto First Aid, Item FAO-310; || Auto First Aid Essentials, Item FAO-340; || Auto First Aid Essentials, Item FDA-532; || Auto First Aid Essentials, Item FDA-552; || Vehicle First Aid Kit, Item 221-U; || Outdoor First Aid Kit, Item FAO-410; || Outdoor First Aid Kit, Item FAO-410 || Outdoor First Aid Kit, Item FAO-420; || Outdoor First Aid Kit, Item FAO-430; || Outdoor First Aid Kit, Item FAO-440; || First Aid & Survival Kit, Item FA-462; || First Aid Kit, FAO-422-06; || First Aid Kit, 403-PC; || First Aid Response Kit, FA-504; || All Purpose First Aid Kit, Item FAO-112; || All Purpose First Aid Kit, Item FAO-122; || All Purpose First Aid Kit, Item FAO-142; || All Purpose First Aid Kit, Item FAO-432; || All Purpose First Aid Kit, Item FAO-444; || All Purpose First Aid Kit, Item FAO-452; || First Aid Essentials, Item FAO-130; || First Aid Essentials, Item FAO-132; || First Aid Essentials, Item FAO-134; || First Aid Essentials, Item FAO-422; || First Aid Essentials, Item FAO-428; || First Aid Essentials, Item FAO-432; || First Aid Essentials, Item FAO-442; || Refillable First Aid Kit, FAO-490C; || Refillable First Aid Kit, FAO-490C; || Brite Stock first aid kits (only labeled on shipping case as being manufactured by First Aid Only): || Item FAO-130-BS; || Item FAO-132-BS; || Item FAO-134-BS; || Manufactured by First Aid Only, Inc. Vancouver, WA. Distributed by Wholesale Merchandisers, Inc., Grand Rapids, MI 49544: || Lake & Trail Outdoor First Aid Kit, Item MJR-420; || Lake & Trail Outdoor First Aid Kit, Item MJR440; || First aid kits labeled DIST. BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544: || meijer First Aid Kit, Item MJR-130; || meijer First Aid Kit, Item MJR-442; || First Aid Kits labeled FIRST AID Exchange: || General Purpose Home First Aid Kit, Item 2800; || Auto First Aid Kit, Item 2825 || First Aid Kit labeled Distributed by Medicine Shoppe International St. Louis, MO: || All purpose First Aid Kit, Item FAO-132-MS || First Aid Kit labeled Mfg. by First Aid Only, Inc. Vancouver, WA Ready Solutions: || First Aid Kit, Item 90030 || First Aid Kit labeled NORTHERN Safety Co., Inc.: || First Aid Kit, Item FAO-442-NS || First Aid Kit labeled Manufactured for: Graham-Field Health Products, Atlanta, Georgia 30060: || Grafco First Aid Kit, Item 1799-9133 and || First Aid Kit labeled -Provided by MOTURIS LTD- || Custom Kit, Item 9099
  • Manufacturer
    First Aid Only Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Distributed under various trade names
Device Recall First Aid Only and First Aid Exchange
  • Modelo / Serial
    Lot Numbers are for kits and cabinets: C0207, C0217, C0227, C0267, C0277, C0287, C0297, C0307, D0027, D0037, D0047, D0057, D0067, D0097, D0107, D0117, D0127, D0137, D0167, D0177, D0187, D0197, D0207, D0247, D0267, E0027, E0047, E0077, E0087, E0177, E0187, D0227, E0297, E0307, E0317, F0017, F0087, F0207, F0267, G0067, G0097, G0137, G0187, G0257, H0017, H0157, H0167, H0237, H0277, H0287, H0297, H0307, H0317, I0047, I0057, I0107, I0127, I0137, I0177, I0187, I0197, I0207, I0217, I0247, I0251, I0277, I0287, J0017, J0037, J0047, J0087, J0097, and J0117.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Worldwide: USA and to one distributor in Dubai, United Arab Emirates.
  • Descripción del producto
    First Aid Only brand cabinets (typically metal wall mount) containing ibuprofen tablets and a variety of other first aid supplies: || Item 249-0/FAO || Item 249-0/P || Item 249-RK/P || First Aid Exchange brand cabinet: || Item 1300-FAE-0103 || Item 1300-FAE-0108 and || Item 1300-PAT-0109
  • Manufacturer
    First Aid Only Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall First Aid Only and First Aid Exchange
Device Recall Dengue IgG ELISA 96 Well Kit
  • Modelo / Serial
    Lot Number: DEG2398, and DEG2488
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    FL, and VA
  • Descripción del producto
    Dengue IgG ELISA 96 Well Kit, Catalog Number: DE050G || The products in question are all Enzyme Linked Immunosorbent Assay (ELISA) Test kits designed and marketed for Research Use Only. || The products in question are all Enzyme Linked Immunosorbent Assay (ELISA) Test kits designed and marketed for Research Use Only.
  • Manufacturer
    Calbiotech Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Dengue IgG ELISA 96 Well Kit
Device Recall Dengue IgM ELISA 96 Well Kit
  • Modelo / Serial
    Lot Number: DEM2514
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    FL, and VA
  • Descripción del producto
    Dengue IgM ELISA 96 Well Kit, Catalog Number: DE051M || The products in question are all Enzyme Linked Immunosorbent Assay (ELISA) Test kits designed and marketed for Research Use Only.
  • Manufacturer
    Calbiotech Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Dengue IgM ELISA 96 Well Kit
Device Recall MilCAM Recon III
  • Modelo / Serial
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    MilCAM Recon III Model Family of IR Imagers that incorporate a Class I infared laser for Laser Range Finding (LRF).
  • Manufacturer
    Flir Systems, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall MilCAM Recon III
Device Recall MilCAM Recon III
  • Modelo / Serial
    Serial numbers: AH0260 AH0264 AH0259 AH0257 AH0250 AH0261 AH0258 AH0467 AH0413 AH0414 AH0415 AH0416 AH0417 AH0450 AH0451 AH0456 AH0458 AH0459 AH0460 AH0462 AH0464 AH0465 AH0461 AH0453 AH0454 AH0452  AH0455 AH0457 AH0463 AH0414 AH0466 AH0468 AH0599 AH0600 AH0606 AH0601 AH0608 AH0597 AH0596 AH0602 AH0470 AH0595 AH0607 AH0471 AH0603 AH0469 AH0609 AH0598 AH0604  AH0605 AH0610 AH0613 AH0611 AH0612, and AH0614.
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution -- Washington, D.C.
  • Descripción del producto
    MilCAM Recon III, Family of IR Imagers that incorporates a Class IIIb infared laser pointer
  • Manufacturer
    Flir Systems, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall MilCAM Recon III
Device Recall Phoenix x/ray analyser series
  • Modelo / Serial
    All affected units.
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Phoenix x/ray analyser series. || Phoenix x|ray analyser series cabinet x-ray systems are used in non-destructive testing, failure analysis, process control, and metrology.
  • Manufacturer
    GE Inspection Technologies, LP
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Phoenix x/ray analyser series
Device Recall Phoenix x/ray inspector series
  • Modelo / Serial
    All affected units.
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Phoenix x/ray inspector series. || Phoenix x|ray inspector series cabinet x-ray systems are used in non-destructive testing, failure analysis, process control, and metrology.
  • Manufacturer
    GE Inspection Technologies, LP
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Phoenix x/ray inspector series
Device Recall Phoenix x/ray v/tome/x series
  • Modelo / Serial
    All affected units.
  • Clase de dispositivo
    Not Classified
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Phoenix x/ray v/tome/x series. || Phoenix x|ray v|tome|x series cabinet x-ray systems are used in non-destructive testing, failure analysis, process control, and metrology.
  • Manufacturer
    GE Inspection Technologies, LP
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Phoenix x/ray v/tome/x series
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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.

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