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Zimmer Manufacturing B.V Recalls
91 recalls on record · July 16, 2014 to May 25, 2016 · Medical Devices
Recalls by year
14
15
16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 56 consists of all product under product code: HWC and same usage: Item no: 47234702032 PERI SCR 3.5MM X 32MM
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 55 consists of all product under product code: HSB and same usage: Item no: 225900132 ONE-PIECE LAG SCREW 11M
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 54 consists of all product under product code: JWH and same usage: Item no: 596009900 NEXGEN TAPER PLUG for
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 53 consists of all product under: product code: JWH and same usage: Item no: 597002501 NEXGEN PRECOAT PEG
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 52 consists of product code: HWC and same usage: Item no: 525004530 NEXGEN OSTEOTOMY CORT BON 525004540 NEXG
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 51 consists of all product under product code: JWH and same usage: Item no: 598603701 NEXGEN OPTION STEMMED
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 50 consists of all product under product code: JWH and same usage: Item no: 595002701 NEXGEN MIS TIBIA PLATE
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 49 consists of all product under product code: JWH and same usage: Item no: 597206529 NEXGEN ALL-POLY PATELL
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 48 consists of all product under product code: JWH and same usage: Item no: 597206526 NEXGEN ALL-POLY PATELL
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 47 consists of all product under product code: LPH and same usage: Item no: 611004022 MODULAR CUP 10 DEGREE
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 46 consists of all product under product code: HWC and same usage: Item no: 114204012 MINI MAGNA-FX CANN SCR
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 45 consists of all product under product code: JWH and same usage: Item no: 511007020 MGII KNEE SLF-TAP BONE
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 44 consists of all product under product code: HWC and same usage: Item no: 114607099 MAGMA-FX CANN SCREW 7.
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 43 consists of all product under product code: HSB and same usage: Item no: 224001016 M/DN R-F IM NAIL 10MM
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 42 consists of all product under product code: HSB and same usage: Item no: 225224010 M/DN FEM IM NAIL 10MM
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 41 consists of all product under product code: KTT and same usage: Item no: 119301042 LAG SCR 12.7D X 100MM
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 40 consists of all product under product code: HSB and same usage: Item no: 225706565 ITST ANTI-ROTATION SCR
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 39 consists of all product under product code: JDI and same usage: Item no: 32902605800 ION IMPLANTED FEM 2
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 38 consists of all product under product code: HSB and same usage: Item no: 225303255 INTERLOCKING IM SCREW
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 37 consists of all product under product code: HSB and same usage: Item no: 225302055 INTERLOCKING IM SCREW
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 36 consists of all product under product code: HSB and same usage: Item no: 225302745 INTERLOCKING IM SCREW
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 35 consists of all product under product code: JWH and same usage: Item no: 522007300 I/B II KNEE FLUTED RO
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 34 consists of all product under product code: JWH and same usage: Item no: 522001700 I/B II KNEE DOMED PATE
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 33 consists of all product under product code: JDI and same usage: Item no: 662406515 HGP II ACETABULAR CUP
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 32 consists of all product under product code: HWC and same usage: Item no: 47115401200 HERBERT BONE SCREW,
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 31 consists of all product under product code: KTT and same usage: Item no: 118113003 FREE-LOCK TUBE & SCP P
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 30 consists of all product under product code: KTT and same usage: Item no: 118100527 FREE-LOCK LAG SCREW, 1
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 29 consists of all product under product code: LPHand same usage: Item no: 32902603800 FEMORAL HEAD +0.5 X 2
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 28 consists of all product under product code: JDI and same usage: Item no: 32902605000 FEMORAL HD 28MM MEDIU
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 27 consists of all product under product code: HSB and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL
Hazard: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.