Category

Medical Devices Recalls

15,654 medical devices recalls on record from CPSC, FDA, and USDA.

15,654 recalls
High RiskFDA
Zimmer Manufacturing B.v.
Product 59 consists of all product under product code: JWH and same usage: Item no: 42540000026 PSN ALL POLY PAT PLY 26MM 42540000029...
Medical Devices·112,588 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 62 consists of all product under product code: LPH and same usage: Item no: 620003620 TRILOGY ACET SHELL 36MM OD MULTI For ...
Medical Devices·400 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 19 consists of all product code: JDI and same usage: Item no: 765301101 CEM FEM ST 11X120 NOCOAT 765301201 CEM FEM ST 12X125 ...
Medical Devices·0 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 35 consists of all product under product code: JWH and same usage: Item no: 522007300 I/B II KNEE FLUTED ROD, 1 for use i...
Medical Devices·49 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 67 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTED 785001200 VERS...
Medical Devices·5,013 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 54 consists of all product under product code: JWH and same usage: Item no: 596009900 NEXGEN TAPER PLUG for use in total knee...
Medical Devices·1,767 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 64 consists of all product under product code: JDI and same usage: Item no: 902605101 UNIPOLAR ENDO FEM HEAD 51MM For use i...
Medical Devices·0 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 3 consists of all products under product code JDI, and same usage: Item no:781803800 12/14 UNIPOLAR FEMORAL HE 781804000 12/14 ...
Medical Devices·2,239 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 15 consists of all product code JDI , and same usage: Item no: 805002802 ASTEL FEM HEAD +0X28MM DI 805002805 ASTEL FEM HEAD ...
Medical Devices·0 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 42 consists of all product under product code: HSB and same usage: Item no: 225224010 M/DN FEM IM NAIL 10MM DIA 225228010 M/...
Medical Devices·1,622 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 43 consists of all product under product code: HSB and same usage: Item no: 224001016 M/DN R-F IM NAIL 10MM DIA 224001018 M/...
Medical Devices·1,102 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 16 consists of all product under poduct code: KWY and same usage: Item no: 500103822 BIPOLAR LINER 38MM OD X 2 500103922 BIP...
Medical Devices·8,773 affected·Jan 11, 2016
High RiskFDA
Varian Medical Systems, Inc.
Eclipse Treatment Planning System versions 11, 13.0, 13.5 and 13.6; Model number: H48; Product Usage: The Eclipse Treatment Planning...
Medical Devices·9,499 affected·Jan 11, 2016
High RiskFDA
Medtronic Neuromodulation
Specify 5-6-5 Lead, Specify 2x8 Lead, Model Numbers: 39565, 39286. Spinal cord stimulation leads. Part of a neurostimulation system for...
Medical Devices·51,138 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 69 consists of all product under product code: JDI and same usage: Item no: 785301701 VERSYS CEMENTED FEM STEM 785301521 VERS...
Medical Devices·13 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 53 consists of all product under: product code: JWH and same usage: Item no: 597002501 NEXGEN PRECOAT PEG TIB PL 597002502...
Medical Devices·202,221 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 63 consists of all product under product code: LPH and same usage: Item no: 620004020 TRILOGY ACET SHELL 40MM O 620004220 TRI...
Medical Devices·2,063 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 70 consists of all product under product code: JDI and same usage: Item no: 785701000 VERSYS HERITAGE FEM STEM 785701100 VERS...
Medical Devices·360 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 66 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTED 785001200 VERS...
Medical Devices·4,353 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 22 consists of all product under product code: JDI and same usage: Item no: 811400218 CPT 12/14 COCR REVISION S 811400318 C...
Medical Devices·16 affected·Jan 11, 2016
High RiskFDA
Zimmer Manufacturing B.v.
Product 71 consists of all product under product code: JDI and same usage: Item no: 783401000 VERSYS PRESS FIT LD/FX ST 783401100 VER...
Medical Devices·2,388 affected·Jan 11, 2016
High RiskFDA
Orthofix, Inc
Firebird Spinal Fixation System Torque Limiting Handle (PN 52-1512) Intended for posterior, non-cervical pedicle, and non-pedicle fixa...
Medical Devices·36 affected·Jan 8, 2016
High RiskFDA
Cook Inc.
Kopans Breast Lesion Localization Needle The Kopans Breast Lesion Localization Needle consists of a bevel-tip needle with centimeter mar...
Medical Devices·134 affected·Jan 8, 2016
High RiskFDA
Natus Medical Incorporated
Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator.
Medical Devices·75 affected·Jan 8, 2016
High RiskFDA
Wfr/aquaplast Corp
Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Breast Device Product Usage: Clear Vue Prone Breast Treatment Ta...
Medical Devices·18 affected·Jan 7, 2016
High RiskFDA
Synthes (usa) Products Llc
Cervical Spine Locking Plate (CSLP) System, 4mm Cancellous Self Tapping Screw, Length 16mm Lot # 9666776 and 4mm Cortex Standard Screw, L...
Medical Devices·30 affected·Jan 6, 2016
High RiskFDA
Global Healthcare Inc
ET-20 Anesthesia Extension Tubes, 2.5 ml approximately, Sterile and Disposable, Wall Medical Inc., Made in China
Medical Devices·2,000 affected·Jan 6, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee Sy...
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee Sy...
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Rymed Technologies, Llc
InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single Use. Products are intended for single patient ...
Medical Devices·46,600 affected·Jan 5, 2016
High RiskFDA
Bard Peripheral Vascular Inc
Bard Distaflo Vascular Bypass Graft; Product Code: DF8006SC; 6 mm x 80 cm. Intended for bypass or reconstruction of peripheral arterial ...
Medical Devices·4 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial K...
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee Sy...
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: Instruments for use with the Oxford Uni Partial...
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Left Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Rymed Technologies, Llc
InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in...
Medical Devices·496,400 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Kn...
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee S...
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Bard Peripheral Vascular Inc
Bard Distaflo Vascular Bypass Graft; Product Code: DF6006SC; 8 mm x 60 cm. Intended for bypass or reconstruction of peripheral arterial ...
Medical Devices·4 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial K...
Medical Devices·72 affected·Jan 5, 2016
High RiskFDA
Biomet U.k., Ltd.
Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Kn...
Medical Devices·72 affected·Jan 5, 2016