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  • Dispositivo 544
  • Fabricante 31827
  • Evento 694
  • Implante 87
Device Recall CIBAVision, CIBASOFT Visitint.
  • Modelo / Serial
    Lot number: 1170119, Expiration: 2007/10, Prescription: base curve 8.9, diameter 13.8, power  -1.50.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. accounts: CA, GA, IL, MN, NJ, TX, VA. Foreign Distributors: Austria, Belgium, Denmark, Finland, France, Germany, Great Britain, Greece, Italy, Luxembourg, Moracco, Netherlands, Norway, Portugal, Spain, South Africa, Sweden, Switzerland and the United Arab Emirates. No government accounts involved.
  • Descripción del producto
    Blue-Vis, CIBASOFT VISITINT, daily wear contact lens. Lot 1170119, Expiration 2007/10, BC 8.9, DIA 13.8, SPH -1.50, CIBA Vision, Corp, Duluth, GA 30097, Made in USA.
  • Manufacturer
    Ciba Vision Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall CIBAVision, CIBASOFT Visitint.
Device Recall Optima
  • Modelo / Serial
    Lot R21000211
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    Nationwide distribution.
  • Descripción del producto
    OPTIMA FW (polymacon) Visibility Tinted Contact Lenses, labeled as -2.25D, 8.7 mm. Responsible firm on the label: Bausch & Lomb Inc., Rochester, NY 14692. || Each box contains six lenses.
  • Manufacturer
    Bausch & Lomb Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Optima
Device Recall FreshLook, TORIC
  • Modelo / Serial
    049007 and 041599
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    01CA, FL, IL, IN, MA, MO, MS, OH, TX, UT, WI; Australia, Canada. There were no government accounts involved. CIBA Vision Canada, Ontario, Canada.
  • Descripción del producto
    FreshLook, TORIC, for Astigmatism (phemfilcon A) Contact Lenses, BC Median, DIA 14.5, Lot 041599, 2007-01Wesley Jessen Corporation, 333 E. Howard Avenue, Des Plains, IL 60018, USA, Made in USA, Sterile.
  • Manufacturer
    Ciba Vision Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall FreshLook, TORIC
Device Recall Katena Products Inc (OEM)
  • Modelo / Serial
    Lot Number: 063207 Exp. 10/2005
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    Ultrakleen KSponge II Spears || Catalog #: K20-5012
  • Manufacturer
    Ultracell Medical Technologies
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Katena Products Inc (OEM)
Device Recall Oasis (OEM)
  • Modelo / Serial
    Lot Numbers: 063203 Exp. 6/2005  063202 Exp. 6/2005   063204 Exp. 7/2005  063206 Exp. 8/2005  063207 Exp 10/2005  063208 Exp 11/2005
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    PVA Foam Surgical Spears || Catalog #: OASIS0525
  • Manufacturer
    Ultracell Medical Technologies
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Oasis (OEM)
Device Recall Graczyk Inc. (OEM)
  • Modelo / Serial
    Lot Number: 062308 Exp. 11/2005
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    Lasik Spears Blunt (5) || Catalog #: U/S32-100
  • Manufacturer
    Ultracell Medical Technologies
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Graczyk Inc. (OEM)
Device Recall Becton Dickinson Microkeratome Blade
  • Modelo / Serial
    Manufacturing Lot Numbers: 959, 962, 964, 965, and 966
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    BD K-3000 Microkeratome Blade || REF 378607
  • Manufacturer
    BD Opthalmic Systems
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Becton Dickinson Microkeratome Blade
Device Recall Glitter Eyes
  • Modelo / Serial
    Green, PID Lot#NA, Button Lot#22940-32, Blue, PID Lot#40523337, Button Lot#22940-32, Bronze, PID Lot#40538359, Button Lot#22940-32, Violet, PID Lot#40522198, Button Lot #22940-32, Green, PID Lot#40581596, Button Lot#22985-95, Blue PID Lot 40550786, Button Lot#22620-19, Blue PID Lot#40505677, Button Lot#22620-20, Bronze PID Lot#40540880, Button Lot#22620-19, Violet, PID Lot#40543810, Button Lot#22620-19.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide, Canada and Puerto Rico.
  • Descripción del producto
    Glitter Eyes (tefilcon), daily wear soft (hydrophilic) contact lenses packed as single units or kits in mulitple glass vials.
  • Manufacturer
    Ciba Vision Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Glitter Eyes
Device Recall Sharpoint ClearTrap Trapezoid Clear Corneal/Implant Knife
  • Modelo / Serial
    Model # 75-2525, Lot #M118200
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    The product was shipped to 2 wholesale accounts in PA and LA.
  • Descripción del producto
    Sharpoint ClearTrap Trapezoid Clear Corneal/Implant Knife. Ophthalmic Knife 2.5 mm x 3.5 mm.
  • Manufacturer
    Surgical Specialties Corp
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Sharpoint ClearTrap Trapezoid Clear Corneal/Implant Knife
Device Recall CIBA Vision contact lens
  • Modelo / Serial
    Lot number 064429, Expiration date, 2006/11
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    The product was distribured to wholesalers located in AL, CA, CO, FL, GA, IA, IL, IN, MA, MO, NC, NJ, NY, OH, OK, OR, PA, TX, UT, WA, and WI.
  • Descripción del producto
    FreshLook Colors (phemfilcon A), 7-day Extended wear soft (hydrophilic) contact lens, Violet, SPH -0.75, Lot 064429, 2006-11, BC: Median DIA: 14-5, Rx only, CIBA Vision Corp., Duluth, GA 30097, USA. The product was distributed in multi-packs (cartons of six lenses each).
  • Manufacturer
    Ciba Vision Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall CIBA Vision contact lens
Device Recall CIBA Vision
  • Modelo / Serial
    Focus Dailies Toric 15 lens pack (Cylinder 10.75/Axis 90¿¿): Sphere -1.00, Lot 2298508; Sphere 1.25, Lot #2298512, 2304513; Sphere -1.50, Lot #2298509, 2304510; Sphere -1.75, Lot #2304512, 2304522 and Sphere -2.00, Lot #2298510. Focus Dailies Toric 30 lens pack (Cylinder -0.75/Axis 90¿¿): Sphere -1.00, Lot #2298475, 2295481, 2298497, 2304509, 2304519, 2304529; Sphere -1.25, Lot #2298480, 2298485, 2298502, 2304523, 2304533; Sphere -1.50, Lot #2298476, 2298482, 2298498, 2304520, 2304530; Sphere -1.75, Lot #2298479, 2298484, 2298501, 2298511, 2304532 and Sphere -2.00, Lot #2298478, 2298483, 2298499, 2304511, 2304521, 2304531.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The product was distributed to various wholesalers (original consignees) Nationwide, Canada and Europe.
  • Descripción del producto
    Focus DAILIES Toric (nelfilcon), One-Day Contact Lenses, Daily Disposable (hydrophilic) soft contact lens, Rx only, Sterile, -1.50, -1.75 x 090, BC 8.6, DIA 14.2, CIBA Vision Corp., Duluth, GA 30097. USA. The product is packaged and distributed as 15 and 30 packs.
  • Manufacturer
    Ciba Vision Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall CIBA Vision
Device Recall Stylus Brand Slit Knife
  • Modelo / Serial
    Model number: 52-2761  Lot/Serial # Exp. Date M262530 2/2008 M262540 3/2008 M262550 3/2008
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide and worldwide. Distribution was to two accounts in the USA and four (4) foreign accounts.
  • Descripción del producto
    2.75 mm Slit Knife, Angled, Bevel Up. Labeled '' Stylus *** 2.75 mm Slit Knife Angled, Bevel, Up***One Unit STERILE R Disposable***Surgical Specialties Corporation***Reading, PA 19606***''
  • Manufacturer
    Surgical Specialties Puerto Rico, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Stylus Brand Slit Knife
Device Recall MAGNIVISION
  • Modelo / Serial
    Product is not coded.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Product was distributed to a a wholesaler in Florida.
  • Descripción del producto
    Product is Magnivision UltraLights reading glasses which have the dioptic power on the label and ''MAGNIVISION AN AMERICAN GREETINGS COMPANY Miramar, FL 33025''
  • Manufacturer
    Magnivision, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall MAGNIVISION
Device Recall Encore and OneVue
  • Modelo / Serial
    There are 768 lot numbers as follows: 3669001157,  3669001465,  3669001756,  3669001960,  3669002711,  3669002714,  3669002816,  3669003208,  3669003214,  3669500011,  3669500414,  3669500514,  3779000756,  3779001722,  3779002117,  3779002513,  3779002911,  3779003020,  3779003624,  3779003906,  3779005316,  3779500013,  3779500120,  3890000722,  3890001706,  3891001712,  3892000954,  3892001402,  3892001414,  3892001712,  3893001417,  3893001611,  3893001711,  3893002612,  3893002613,  3893002712,  3893003020,  3893003107,  3893003302,  3893003614,  3893004706,  3893004806,  3893500111,  3893500702,  3893500802,  3893500902,  3894001058,  3894001560,  3894001654,  3894002213,  3894002607,  3894002610,  3894002811,  3894003005,  3894004306,  3894004502,  3894004904,  3894005004,  3894500205,  3894500310,  3894500311,  3894500313, 3894500402,  3894500411,  3894500511,  3894500704,  3894500706,  3895001456, 3895002758,  3895002855,  3895003024,  3895003220,  3895003315,  3895003320, 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 3904002060,  3904002313,  3904003018,  3904003102,  3904003202,  3904003204,  3904500002,  3904500103,  3904500203,  3904500213,  3904500305,  3905001157,  3905001257,  3905001665,  3905001852,  3905002026,  3905002056,  3905003321,  3905004115,  3905004260,  3905004455,  3905004505,  3905004615,  3905004705,  3905004911,  3905004914,  3905005011,  3905005014,  3905005111,  3905005114,  3905005124,  3905005602,  3905005702,  3905005724,  3905005802,  3905006316,  3905006416,  3905007506,  3905007812,  3905500017,  3905500105,  3905500117,  3905500210,  3905500410,  3905500411,  3905500414,  3905500515,  3905500607,  3905500616,  3905500708,  3905500716,  3905500720,  3905501004,  3906001552,  3906002614,  3906002714,  3907001260,  3907003006,  3907003511,  3907003607,  3907003614,  3907003714,  3907003716,  3907003816,  3907004112,  3907004308,  3907004424,  3907004524,  3907005410,  3907005710,  3907500011,  3907500210,  3907500324,  3911001411,  3912001262,  3912001265,  3912001905,  3912002224,  3912003400,  3912003611,  3912004007,  3912004107,  3912004207,  3912500011,  3912500107,  3913001255,  3913001460,  3913001462,  3913002205,  3913002814,  3913002910,  3913003010,  3913003110,  3913500105,  3913500205,  3913500308,  3914001462,  3914001923,  3914002155,  3914002165,  3914002255,  3914003160,  3914003311,  3914003322,  3914003411,  3914004513,  3914004524,  3914004613,  3914004624,  3914004907,  3914005007,  3914005116,  3914005205,  3914005305,  3914005405,  3914005505,  3914005605,  3914006614,  3914006702,  3914006703,  3914006902,  3914007408,  3914007508,  3914007508,  3914500011,  3914500105,  3914500111,  3914500205,  3914500308,  3914500313,  3914500413,  3914500903,  3915000862,  3915001060,  3915001265,  3915001453,  3915001455,  3915001654,  3915002605,  3915500065,  3915500205,  3916000851,  3916002513,  3916002602,  3916002702,  3916005504,  3916500204,  3921001051,  3921003118,  3921003218,  3921004000,  3921004024,  3921004124,  3921004212, 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 4343008014,  4343008306,  4343008406,  4343008512,  4343008612,  4343008710,  4343008920,  4343009010,  4343010916,  4343500007,  4343500160,  4343500320,  4344002109,  4344004100,  4344500265,  4344500304,  4344500355,  4344500365,  4344500455,  4344500465,  4345002513,  4345003120,  4350001060,  4350002409,  4350002712,  4351002206,  4351500060,  4351500106,  4351500112,  4351500160,  4351500212,  4352001060,  4352003708,  4352003808,  4352003912,  4352004012,  4352006500,  4352006600,  4352006700,  4352500008,  4352500160,  4353002220,  4353002706,  4353003000,  4353003200,  4353500160,  4354003012,  4360001155,  4360002814,  4360002914,  4360003808,  4360500108,  4360500109,  4360500110,  4361002665,  4361004724,  4361004824,  4361004920,  4361005024,  4361005109,  4361005216,  4361005712,  4361005804,  4361005911,  4361006008,  4361006010,  4361006210,  4361006510,  4361006700,  4361006800,  4361500009,  4361500016,  4361500120,  4361500300,  4361500365,  4361500455,  4361500555,  6591001465,  6591001960,  6598002213,  6598002611,  6599002855,  6599003315,  6599003414,  6599004312,  6599005904,  6608004355,  6608004911,  6608005602,  6608007108,  6609000960,  6616001460,  6616002205,  6616002910,  6617002155,  6617003411,  6617007408,  6617500005,  6617500005,  6618001355,  6626001960,  6626005005,  6626008920,  6626010916,  6627001455,  6627004100,  6627500065,  6634001805,  6634001905,  6635003205,  6635003708,  6635006600,  6636001255,  6636003000,  6636003200,  6636500006,  6636500006,  6643001155,  6643001265,  6643002814,  6644002665,  6644002955,  6644004724,  6644005020,  6644005712,  6644005712,  6644005804,  6644006110,  6644006700,  9198000601,  9198000613,  9198000712,  9198000812,  9199000713,  9201000313,  9215001213,  9215001712,  9215001812,  9215001912,  9215002012,  9801001851,  9804001706,  9807003614,  9809003320,  9811002224,  9814001610,  9818001157,  9818001864,  9820004524,  9825004007,  9838003516,  9843002409,  9844001905,  9853002305,
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Coopervision, Scottsville, NY is recalling from domestic customers nationwide. Product in Canada and Europe being recalled by affiliate in Europe.
  • Descripción del producto
    SOFT CONTACT LENSES (toric) packaged under the following labels: (1) CV \ ENCORE toric (methafilcon A) || and (2) ONEVUE 55 toric (methafilcon A) flexible wear. || Responsible firm on label: Coopervision, Hamble, SO31, 4RF, UK, Scottsville, NY 14546, USA *** Made in UK. The lenses are sold in boxes of 6 and sold individually as trial lenses.
  • Manufacturer
    Coopervision Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Encore and OneVue
Device Recall Frequency 55
  • Modelo / Serial
    1468-212, Exp. 10/2008
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide. 33 eye care practitioners in the following states: AR, AL, CA, DE, FL, GA, IA, KS, MI, MA, NJ, NY, NC, OH, OK, PA, TX, UT, VA, and WI. Lenses were also shipped to Coopervision affiliates in the United Kingdom and Canada.
  • Descripción del producto
    Frequency 55 Toric (methafilcon B), flexible wear contact lenses (tinted). Responsible firms on the label: CooperVision ** Hamble, SO31 4RF, UK ** Scottsville, NY 14546.
  • Manufacturer
    Coopervision Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Frequency 55
Device Recall Alcon Ladarwave
  • Modelo / Serial
    Serial Numbers: LWN1002Z LWN1003Z LWN1010Z LWN1011Z LWN1013Z LWN1023Z LWN1025Z LWN1035Z LWN1040Z LWN1440Z LWN1513Z LWN1522Z LWN1626Z LWN1629Z LWN1647Z LWN1748Z LWN1796Z LWN1805Z LWN1817Z LWN1820Z LWN1821Z LWN1822Z LWN1823Z LWN1843Z LWN1846Z LWN1944Z LWN1945Z LWN1946Z LWN1947Z LWN1949Z LWN1950Z LWN1952Z LWN1953Z LWN1954Z LWN1955Z LWN1956Z LWN1957Z LWN1958Z LWN1959Z LWN1961Z LWN2187Z LWN2188Z LWN2189Z LWN2190Z LWN2191Z LWN2192Z LWN2193Z LWN2194Z LWN2197Z LWN2198Z LWN2199Z LWN2200Z LWN2262Z LWN2263Z LWN2264Z LWN2265Z LWN2267Z LWN2268Z LWN2269Z LWN2270Z LWN2271Z LWN2272Z LWN2273Z LWN2276Z LWN2277Z LWN2278Z LWN2279Z LWN2280Z LWN2342Z LWN2343Z LWN2344Z LWN2345Z LWN2346Z LWN2347Z LWN2348Z LWN2349Z LWN2350Z LWN2351Z LWN2352Z LWN2353Z LWN2355Z LWN2356Z LWN2357Z LWN2403S LWN2404S LWN2405S LWN2406S LWN2414Z LWN2415Z LWN2416Z LWN2417Z LWN2420Z LWN2421Z LWN2427S LWN2428S LWN2464Z LWN2465Z LWN2466Z LWN2467Z LWN2468Z LWN2469Z LWN2470Z LWN2471Z LWN2472Z LWN2473Z LWN2475Z LWN2476Z LWN2477Z LWN2478Z LWN1609Z LWN1951Z
  • Clasificación del producto
    Ophthalmic Devices
  • Distribución
    109 U.S. customers and 48 international device locations. There were 12 devices on-hand.
  • Descripción del producto
    Alcon Ladarwave CustomCornea Wavefront System'' Aberrometer software Version 7.91
  • Manufacturer
    Alcon Laboratories, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Alcon Ladarwave
Microflow Needles, catalog #DP8200, with 0 degree tapering, labeled in part ***Non-sterile, Manuf...
  • Modelo / Serial
    Julian date coded ''2003163''
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Product was sold to 6 direct accounts in FL, IA, WI, MA and IL. Product was additionally sold to 4 international distributors.
  • Descripción del producto
    Microflow Needles, catalog #DP8200, with 0 degree tapering, labeled in part ***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box.
  • Manufacturer
    Bausch & Lomb Incorporated
  • 1 Event
    • Retiro De Equipo (Recall) de Microflow Needles, catalog #DP8200, with 0 degree tapering, labeled in part ***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box.
Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in part***Non-sterile, Manuf...
  • Modelo / Serial
    Julian date coded ''2003163''
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Product was sold to 6 direct accounts in FL, IA, WI, MA and IL. Product was additionally sold to 4 international distributors.
  • Descripción del producto
    Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in part***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box.
  • Manufacturer
    Bausch & Lomb Incorporated
  • 1 Event
    • Retiro De Equipo (Recall) de Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in part***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box.
Device Recall Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled
  • Modelo / Serial
    M190500 exp 11/2007 and M203840 exp 12/2007
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    The products were shipped to two hospitals in CA, two sales representatives in NC & IL, and three wholesalers in IL, Belgium, Canada, and Austrailia.
  • Descripción del producto
    Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled. The product can be sold as an individual unit or in a box of 6 knives.
  • Manufacturer
    Surgical Specialties Corp
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled
Device Recall CX9625 Light Pipe (25 Gauge).
  • Modelo / Serial
    Lot numbers: 207089, 209102, 02121321, 02171838, 02192048, 02212272, 02222332, 02242552, 02262741, 02272856, 02293066, 02313269, 02323381, 02333458, 02363752, 02383927, 02404141, 02414225, 02424507, 02434421, 02434520, 02444529, 02454627, 02454672, 02464725, 02474823, 02484921, 02505121, 03020326, 03040522, 03040669, 03060728, 03060803, 03060865, 03080924, 03101124, 03111222, 03131428, 03151624, 03171820, 03171998, 03192023, 03212226, 03212370, 03232422, 03242537, 03252628, 03262726, 03303276, and 03303313.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The product was shipped to hospitals/medical facilities and physicians in AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NJ, NH, NY, NC, OH, PA, TN, TX, UT, VA, WA, WI, and WV. Nationwide. The product was also shipped to Puerto Rico, Argentina, Australia, Brazil, Canada, China, Hong, Kong, India, Japan, Korea, Malaysia, Mexico, New Zealand, The Netherlands, Philippines, Singapore, Spain, Taiwan, and Thailand.
  • Descripción del producto
    CX9625 Light Pipe (25 Gauge). The product is sold in packs containing six pipes.
  • Manufacturer
    Bausch & Lomb Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall CX9625 Light Pipe (25 Gauge).
Device Recall IPSAN patient bracelet
  • Modelo / Serial
    All lots of the German translated patient bracelets
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    Germany, Switzerland, and Austria
  • Descripción del producto
    ISPAN patient bracelet, given to patients post surgery to warn of further use of dinitrogen monoxide
  • Manufacturer
    Alcon Laboratories, Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall IPSAN patient bracelet
Model LightLas 532 Opthalmic Photocoagulator Laser
  • Modelo / Serial
    All codes
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    CA, GA
  • Descripción del producto
    Model LightLas 532 Opthalmic Photocoagulator Laser
  • Manufacturer
    LightMed USA Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Model LightLas 532 Opthalmic Photocoagulator Laser
Device Recall Healon GV
  • Modelo / Serial
    Lots: #5047293 and #5048892
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    The product was distributed to customers in OH and PA.
  • Descripción del producto
    Healon GV, 14 mg per mL, Sodium Hyaluronate, 0.55 ml each, supplied with sterile single-use cannula, Rx only, Manufactured by Pharmacia AB Sweden for Pharmacia & Upjohn Company, A subsidiary of Pharmacia Corporation, Kalamazoo, MI 49001 USA, MADE IN SWEDEN.
  • Manufacturer
    Cardinal Health
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Healon GV
MicroSTAAR Injector Cartridges Models: || SFC-25 (utilized with plate haptic Collamer lens) || MT...
  • Modelo / Serial
    SFC-25 (8 lots) 1180608, 1181078, 1181170,1181171, 1181396, 1181397, 1182237, 1184864 MTC-60 (25 lots) 1177222, 1177950, 1178121, 1178212, 1176868, 1177421, 1178738, 1178883, 1178885, 1179023, 1181789, 1181790, 1181797, 1181798, 1181980, 1182245, 1182342, 1182343, 1182344, 1182345, 1182675, 1182676, 1182677, 1182761.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide, Canada and Australia
  • Descripción del producto
    MicroSTAAR Injector Cartridges Models: || SFC-25 (utilized with plate haptic Collamer lens) || MTC-60 (utilized with plate haptic Silicone lens)
  • Manufacturer
    Staar Surgical Co Inc
  • 1 Event
    • Retiro De Equipo (Recall) de MicroSTAAR Injector Cartridges Models: || SFC-25 (utilized with plate haptic Collamer lens) || MTC-60 (utilized with plate haptic Silicone lens)
Device Recall CVS Brand
  • Modelo / Serial
    All lot codes
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    CVS Pharmacy One Step Cleaning & Disinfecting Solution No Rub, For soft contact lenses (hydrophilic) replaced in 30 days or less. Contains hydrogen peroxide as the disinfecting agent. 12 Fl. Oz (355 ML). || [OTC] || Item Number: 191648
  • Manufacturer
    CVS
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall CVS Brand
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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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La International Medical Devices Database está bajo la licencia Open Database License y sus contenidos bajo la licencia Creative Commons Attribution-ShareAlike . Al usar esta data, siempre citar al International Consortium of Investigative Journalists. Puede descargar acá una copia de la base de datos.

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