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Vista de la lista Vista de las tarjetas
  • Dispositivo 544
  • Fabricante 31827
  • Evento 694
  • Implante 87
Amvisc PLUS - PREPARATION viscoelastic STERILE - registration 10196150045 - Lots D090105D D100009...
  • Modelo / Serial
  • Clasificación del producto
    Ophthalmic Devices
  • Manufacturer
    BL INDÚSTRIA OTICA LTDA
  • 1 Event
    • Alerta De Seguridad para Amvisc PLUS - PREPARATION viscoelastic STERILE - registration 10196150045 - Lots D090105D D100009A, D100011A, D100016A, D100016B, D100016C, D100026C, D100044D, D100060A, D100060B, D100080A, D100081A, D110015A, D110045A, D110046A, D110070A, D110071A, D110072A, D110091A, D110091A, 024028
Avaira and BioComfort XO contact lenses
  • Modelo / Serial
  • Clasificación del producto
    Ophthalmic Devices
  • Descripción del producto
    Press release: Recall of Avaira and BioComfort XO contact lense
  • Manufacturer
    CooperVision
  • 1 Event
    • Alerta De Seguridad para Avaira and BioComfort XO contact lenses
Avaira / Cadence Evolve / Options Evolve / Enfilcon Dk100 Aspheric
  • Modelo / Serial
    L46 - Avaira Sphere
  • Clasificación del producto
    Ophthalmic Devices
  • Descripción del producto
    MD: Contact lens, vision corrective, reusable
  • Manufacturer
    CooperVision Inc.
  • 1 Event
    • Notificaciones De Seguridad De Campo acerca de Avaira / Cadence Evolve / Options Evolve / Enfilcon Dk100 Aspheric
avaira sphere contact lenses.
  • Modelo / Serial
  • Clasificación del producto
    Ophthalmic Devices
  • Manufacturer
    CooperVision
  • 1 Event
    • Notificaciones De Seguridad De Campo acerca de avaira sphere contact lenses.
Avaira Sphere contact lenses
  • Modelo / Serial
  • Clasificación del producto
    Ophthalmic Devices
  • Manufacturer
    CooperVision Manufacturing Ltd.
  • 1 Event
    • Alerta De Seguridad para Avaira Sphere contact lenses
avaira toric and biocomfort xo toric contact lenses
  • Modelo / Serial
  • Clasificación del producto
    Ophthalmic Devices
  • Descripción del producto
    Press release: Recall of Avaira Toric and BioComfort XO Toric contact lenses
  • Manufacturer
    CooperVision
  • 1 Event
    • Alerta De Seguridad para avaira toric and biocomfort xo toric contact lenses
AVAIRA Toric contact lenses
  • Modelo / Serial
  • Clasificación del producto
    Ophthalmic Devices
  • Descripción del producto
    ophthalmological technology
  • Manufacturer
    CooperVision
  • 1 Event
    • Notificaciones De Seguridad De Campo acerca de AVAIRA Toric contact lenses
Avaira Toric daily contact lenses
  • Modelo / Serial
  • Clasificación del producto
    Ophthalmic Devices
  • Descripción del producto
    Press release: Suspend use of Avaira Toric daily contact lenses advisable
  • Manufacturer
    CooperVision
  • 1 Event
    • Alerta De Seguridad para Avaira Toric daily contact lenses
Battery-operated Cautery || High Temperature, fine/Loop/ Vasectomy Tip
  • Modelo / Serial
    Sterile lot numbers: 0104E 0204B 0204C 0204E 0304A 0304C 0404A 0404C 0404H 0404J 0404G 0504A 0504F 0204A 0304E 0504B 0204D 0504D 0504C 0504E 0504F. EXP DATES 2/1/08-5/1/04
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed to: 291 accounts in the USA, 8 in Canada, 18 in Europe, 1 in the Middle East, 1 in Asia, 4 in the Pacific Rim 1 in Africa and 5 US goverment/Military.
  • Descripción del producto
    Battery-operated Cautery || High Temperature, fine/Loop/ Vasectomy Tip
  • Manufacturer
    Aaron Medical Industries, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Battery-operated Cautery || High Temperature, fine/Loop/ Vasectomy Tip
Battery-operated Cautery || Low Temperature, fine/elongated Tip
  • Modelo / Serial
    Sterile lot numbers: 0204B 0204D 0204E 0304A 0304C 0304D 0404A 0404E 0404G 0404H 0404J 0504A 0504C 0504E 0504F. EXP DATES 2/1/08-5/1/04
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed to: 291 accounts in the USA, 8 in Canada, 18 in Europe, 1 in the Middle East, 1 in Asia, 4 in the Pacific Rim 1 in Africa and 5 US goverment/Military.
  • Descripción del producto
    Battery-operated Cautery || Low Temperature, fine/elongated Tip
  • Manufacturer
    Aaron Medical Industries, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Battery-operated Cautery || Low Temperature, fine/elongated Tip
Bausch and Lomb ReNu with MoistureLoc Multi-Purpose Solution
  • Modelo / Serial
  • Clasificación del producto
    Ophthalmic Devices
  • Descripción del producto
    Bausch and Lomb ReNu with MoistureLoc Multi-Purpose Solution
  • Manufacturer
    manufacturer #28616
  • 1 Event
    • Notificaciones De Seguridad De Campo acerca de Bausch and Lomb ReNu with MoistureLoc Multi-Purpose Solution
Bausch & Lomb, Biotrue
  • Modelo / Serial
    Lot GK2127 (twin packs), SKU: 623588, GK2131 (twin packs), SKU: 623500, STL2019, (6 pk shelf display containing GK2131, SKU: 629743 and STL2025 (6 pk shelf display containing GK2127), SKU: 629743.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Nationwide.
  • Descripción del producto
    Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile.
  • Manufacturer
    Bausch & Lomb Inc- Greenville Solutions Plant
  • 1 Event
    • Retiro De Equipo (Recall) de Bausch & Lomb, Biotrue
Bausch & Lomb Boston Conditioning Solution, Original Formula
  • Modelo / Serial
    All lots
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. Nationwide, Canada and Hong Kong
  • Descripción del producto
    Bausch & Lomb Boston¿ Conditioning Solution, Original Formula, Bausch & Lomb Incorporated, Rochester, NY 14609. The product is packed in 1 fl oz (30 mL), 3 fl oz (90 mL), 3.5 fl oz (105 mL) and 4 fl oz (120 ml) bottles.
  • Manufacturer
    Bausch & Lomb Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Bausch & Lomb Boston Conditioning Solution, Original Formula
Bausch Lomb PeroxiClear Peroxide Solution
  • Modelo / Serial
    Item #623815, UPC: 310119038154, Lot number: GE15012ST, Lot Exp. Date: 2016/11/30, Lot number: GF15055ST, Lot Exp. Date: 2016/12/31, Lot numbers: GH15053R, GH15056-1, GH15067ST, GH15070ST, GH15076ST, GH15081ST and  GH15086-1, Lot Exp. Date: 2017/02/28, Lot numbers: GK15116ST, GK15118A1, Lot Exp. Date: 2017/04/30, Lot numbers: GL15148-1 and GL15148-2, Lot Exp. Date: 2017/05/31, Lot number: GC16080-1, Lot Exp. Date: 2017/09/30 and 623815C (3 oz.), Lot numbers: GE16060A1 and GE16066-1, Lot Exp. Date: 2017/11/30; Item #623816 (12oz.), UPC 310119038161, Lot numbers: GC15002ST, GC15008ST, GC15008ST1 and GC15012AST, Lot Exp Date: 2016/09/30, Lot numbers: GD15100ST1, GD15115AST, GD15124ST and GD15124ST2, Lot Exp Date: 2016/10/31, Lot numbers: GE15132ST and GE15156ST, Lot Exp Date: 2016/11/30, Lot numbers: GF15110ST and GF15110ST1, Lot Exp Date: 2016/12/31, Lot numbers: GG15023STR, GG15038ST and GG15044ST, Lot Exp Date: 2017/01/31, Lot numbers: GH15036ST, GH15039ST, GH15045ST and GH15128ST, Lot Exp Date: 2017/02/28, Lot numbers: GJ15070ST and GJ15081ST, Lot Exp Date: 2017/03/31, Lot numbers: GK15129ST and GK15131ST, Lot Exp Date: GL15004STR, GL15012ST and GL15048ST, Lot Exp Date: 2017/05/31, Lot numbers: GM15027AST, GM15034ST, GM15041ST and GM15044ST, Lot Exp Date: 2017/06/30, Lot numbers: GA16023ST1, GA16052ST and GA16056ST, Lot Exp Date: 2017/07/31, Lot numbers: GC16035ST, GC16044ST and GC16060ST, Lot Exp Date: 2017/09/30, Lot numbers: GE16001ST, GE16004ST, GE16009ST and GE16009ST1, Lot Exp Date: 2017/11/30, Lot numbers: GF16087ST and GF16087ST1, Lot Exp Date: 2017/12/31, Lot number: GG16003ST, Lot Exp Date: 2018/01/31 and 623816B, UPC 310119038161, Lot number: GG16116ST, Lot Exp Date: 2017/10/31; Item #623817 (12 oz. Twin Pack), UPC 310119038178, Lot number: GC15026ST, Lot Exp Date: 2016/09/30, Lot numbers: GD15095ST, Lot Exp Date: 2016/10/31, Lot numbers: GE15131ST, GE15133ST, GE15149ST and GE15161AST, Lot Exp Date: 2016/11/30, Lot number: GF15107ST1, Lot Exp Date: 2016/12/31, Lot numbers: GG15002STR and GG15037ST, Lot Exp Date: 2017/01/31, Lot numbers: GH15037ST, GH15038ST, GH15122ST and GH15132ST, Lot Exp Date: 2017/02/28, Lot numbers: GJ15078ST, GJ15094ST and GJ15104ST, Lot Exp Date: 2017/03/31, Lot numbers: GK15136ST, GK15142ST and GK15147ST, Lot Exp Date: 2017/04/30, Lot numbers: GL15046ST and GL15054ST, Lot Exp Date: 2017/05/31, Lot numbers: GM15037ST and GM15048ST, Lot Exp Date: 2017/06/30, Lot numbers: GA16027ST, GA16032ST, GA16036ST, GA16043ST, GA16046ST and GA16060ST, Lot Exp Date: 2017/07/31, Lot number: GC16049ST, Lot Exp Date: 2017/09/30, Lot numbers: GE16013ST, GE16014ST, GE16030ST and GE16033ST, Lot Exp Date: 2017/11/30 and Lot number: GF16083STR1, Lot Exp Date: 2017/12/31; Item #623908 (Target), UPC 310119039083, Lot number: GD15100ST, Lot Exp Date: 2016/10/31, Item #623910 (Walmart), UPC 310119039106, Lot numbers: GD15124ST1, Lot Exp Date: 2016/10/31. Lot number: GJ15084ST, Lot Exp Date: 2017/03/31; Item #629712 (Starter Kit), UPC 310119097120, Lot numbers: GC15037ST, GC15044ST, GC15044ST1, GC15049ST and GC15052ST Lot Exp. Date: 2016/09/30, Lot numbers: GD15133-1, GD15139ST and GD15144ST, Lot Exp. Date: 2016/10/31, Lot numbers: GE15016ST, GE15021ST and GE15028ST, Lot Exp. Date: 2016/11/30, Lot numbers: GF15006ST, GF15018ST, GF15050AST, GF15052ST, GF15060ST, GF15064ST, GF15071ST, GF15075-1 and GF15084ST, Lot Exp. Date: 2016/12/31, Lot numbers: GH15105ST, GH15107ST, GH15108ST, GH15109ST and GH15120ST, Lot Exp. Date: 2017/02/28, Lot numbers: GK15090ST, GK15092ST, GK15095ST, GK15100ST, GK15106ST and GK15118ST, Lot Exp. Date: 2017/04/30, Lot numbers: GL15160ST and GL15163ST, Lot Exp. Date: 2017/05/31, Lot numbers: GM15001ST, GM15005ST, GM15011-1 and GM15020-1, Lot Exp. Date: 2017/06/30, Lot numbers: GA16072-1 and GA16076-1, Lot Exp. Date: 2017/07/31, Lot number: GC16075-1, Lot Exp. Date: 2017/09/30 and Lot numbers: GE16048-1, GE16048-3, GE16052-1 and GE16057-1, Lot Exp. Date: 2017/11/30.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-U.S. Nationwide and country of: Canada.
  • Descripción del producto
    PeroxiClear Peroxide Solution, (3oz. and 12 oz., 12 oz. Twin Pack, 2x12 oz. Twin Pack for Target stores, 12 oz. for Walmart Vision Center and 3 oz. Starter Kit US), Manufactured by Bausch + Lomb, Rochester, NY 14609. || PeroxiClear 3% Hydrogen Peroxide Cleaning & Disinfecting Solution is indicated for the daily cleaning, removal of protein deposits, disinfection and storage of soft (hydrophilic) contact lenses (including silicone hydrogel) and rigid gas permeable contact lenses.
  • Manufacturer
    Bausch & Lomb Inc Irb
  • 1 Event
    • Retiro De Equipo (Recall) de Bausch Lomb PeroxiClear Peroxide Solution
Bausch & Lomb ReNu
  • Modelo / Serial
    Lot Number GA8028.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distribution: Nationwide, Trinidad, St. Croix, St. Thomas, Aruba and Bermuda.
  • Descripción del producto
    Bausch & Lomb ReNu¿ Multi-Purpose Solution, 12 fl.oz. (355 ml), Bausch & Lomb, Incorporated, Rochester, NY 14609. || Product is used for For the cleaning, rinsing, disinfecting, and storage of soft contact lenses.
  • Manufacturer
    Bausch & Lomb Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Bausch & Lomb ReNu
BD 1 OVD Sodium Hyaluronate
  • Modelo / Serial
    Lot No. Exp. Date RDOl71B 2012-12; RD0070A 2012-05; RD0018A 2012-02; RD0007A 2012-01 RC0064C 2011-06; RC0004A 2011-01;
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Beaver-Visitec International (Beaver-Visitec) BD 1% OVD Sodium Hyaluronate, 10 mg/ml 1.0 mL. Sterile. Rx || For Intraocular Use || REF 585304 || Use as a surgical aid to protect corneal endothelium during cataract extraction procedures, intraocular lens implantation and anterior segment surgery.
  • Manufacturer
    Becton Dickinson and Company
  • 1 Event
    • Retiro De Equipo (Recall) de BD 1 OVD Sodium Hyaluronate
BD Microkeratome K3000 and K4000
  • Modelo / Serial
    All serial numbers
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide
  • Descripción del producto
    BD Microkeratome K3000 and K4000;Catalog Number: 378660, Becton Dickinson & Company (BD)
  • Manufacturer
    Becton Dickinson and Company
  • 1 Event
    • Retiro De Equipo (Recall) de BD Microkeratome K3000 and K4000
BD Ophthalmic
  • Modelo / Serial
    Lot Number: 8018591
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    AZ, CA, CO, IL, OH, FL, PA , TN, TX,and VA Foreign: Australia and Japan.
  • Descripción del producto
    BD Visitec High Viscosity Injector, 4mm || Ref: 585173. The product is intended for Vitroretinal Surgery.
  • Manufacturer
    Becton Dickinson and Company
  • 1 Event
    • Retiro De Equipo (Recall) de BD Ophthalmic
BD Visitec
  • Modelo / Serial
    Lot Numbers: 3182770, 3231212, 3234243, 3238890, 3274064, 3281592, 3318026, 3325843, 3330607, 3344597, 3344633, 4012982, 4033079, 4049076, 4069650, 4084089, 4084102, 4106845, 4125046, 4141947, 4147817
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    BD EdgeAhead Stiletto/MVR Knife 1.1mm (19g) || REF 585240
  • Manufacturer
    BD Opthalmic Systems
  • 1 Event
    • Retiro De Equipo (Recall) de BD Visitec
BD Visitec EdgeAhead MVR Knife
  • Modelo / Serial
    Model # 585230, Lot 9202221
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- United States, Canada and Japan.
  • Descripción del producto
    BD Visitec EdgeAhead MVR Knife, BD Opthalmic Systems, Waltham, MA. || Intended for use in cataract surgery to create self-sealing stab incisions through the cornea or sclera. Also used in retinal surgery for sclerotomy incisions.
  • Manufacturer
    Becton Dickinson and Company
  • 1 Event
    • Retiro De Equipo (Recall) de BD Visitec EdgeAhead MVR Knife
Biofinity XR Toric
  • Modelo / Serial
    Exp. date 2017-07-11; Lots: R12497769, R12519016, R12508969, R12496191, R12514162, R12518889, R12483347, R12518980, R12496182, R12496192, R12498168, R12502974, R12496166, R12496196, R12501147, R12508370, R12518890, R12518978.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    USA Distribution
  • Descripción del producto
    Biofinity XR Toric contact lenses 8.7/14.5 - 6PK || Biofinity XR Toric (comfilcon A) Soft (Hydrophilic) Contact Lenses are indicated for the correction of ametropia (myopia or hyperopia) with astigmatism) in aphakic and non-aphakic persons with non-diseased eyes in powers from -20.00 to +20.00 diopters and astigmatic corrections from -0.25 to -5.75 diopters. The Biofinity (comfilcon A) Soft (Hydrophilic) Contact Lenses have been approved for extended wear for up to 6 nights /7 days of continuous wear. It is recommended that the contact lens wearer first be evaluated on a daily wear schedule. If successful, then a gradual introduction of extended wear can be followed as determined by the prescribing Eye Care Practitioner.
  • Manufacturer
    CooperVision Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Biofinity XR Toric
Biomedics Toric
  • Modelo / Serial
    Lots # 8246525202 & 8255525096
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution.
  • Descripción del producto
    Soft Contact Lens
  • Manufacturer
    Cooper Vision Caribbean Corp.
  • 1 Event
    • Retiro De Equipo (Recall) de Biomedics Toric
Biotrue ONEday (nesofilcon A) lenses
  • Modelo / Serial
    Select -2.25/-3.00 Diopter Lot Numbers: W57209820 (exp. date 05/19/2019), W57210174 (exp. date 05/23/2019), W57210440 (exp. date 05/28/2019), W57211652 (exp. date 06/09/2019), W57211916 (exp. date 06/09/2019), W57212210 (exp. date 06/09/2019), W57212440 (exp. date 06/09/2019),  W57212697 (exp. date 06/09/2019), W57212926 (exp. date 06/09/2019), W57213158 (exp. date 06/09/2019), W57213453 (exp. date 06/09/2019), W57213743 (exp. date 07/01/2019), W57213969 (exp. date 07/01/2019), W57214208 (exp. date 07/01/2019), W57214459 (exp. date 07/01/2019),  W57214717 (exp. date 07/01/2019), W57215039 (exp. date 07/01/2019), W57215293 (exp. date 07/01/2019), W57215517 (exp. date 07/01/2019), W57215783 (exp. date 07/01/2019).
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed US (nationwide), Canada, Japan and Thailand.
  • Descripción del producto
    BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A), Product Order Number Biotrue SVS - 7201, STERILE, Rx Only; The lenses are available in 5 pack, 30 pack and 90 pack sizes; Biotrue ONEday Foil - Part Number 8098001, Biotrue ONEday 5 pack Carton International - Part Number 8101403, and Biotrue ONEday 90 pack Carton International - Part Number 8098203.
  • Manufacturer
    Bausch & Lomb Inc Irb
  • 1 Event
    • Retiro De Equipo (Recall) de Biotrue ONEday (nesofilcon A) lenses
Boston ES Rigid Gas Permeable Contact lens
  • Modelo / Serial
    Lot Number: 156PTC05.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution -- TX, IN and WI.
  • Descripción del producto
    Boston ES Rigid Gas Permeable Contact lens manufactured with Fluoro Silicone Acrylate Rigid Gas Permeable Contact Lens Material. Bausch & Lomb, Inc. Wilmington, MA 01887. || Indicated for daily wear for the correction of refractive ametropia in aphakic and/or not-aphakic persons with non-diseased eyes.
  • Manufacturer
    Bausch & Lomb Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Boston ES Rigid Gas Permeable Contact lens
Cataract Pack
  • Modelo / Serial
    Lot numbers 140513353 140613850 140714553 140814881 140815097
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Distribution to Florida, New York and Puerto Rico..
  • Descripción del producto
    Cataract Pack, Catalog # 900-944 || Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.
  • Manufacturer
    Customed, Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Cataract Pack
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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.