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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.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone screw 4.5x50 selftap 00625004550 Bone scr
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp ii acetabular cup bone screw selftap 6.5x20mm 0066240
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls VersaFx Femoral Fixation System Hex head compression screw 4.7 mm dia. 2 inch (51 mm) length 47116202400
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical screw, 3.5 mm hex head, 57 mm length 00225305
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 45 mm Length 47115504507 Herbert Cannulated Bone Screw S
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Mini MagnaFx Cannulated Screw Fixation System Small Cannulated Bone Screw, Fully Threaded, 5.0 mm Diameter, 20 mm Length
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 45 mm Length 00225304542 M/DN Intramedull
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Zimmer Plates and Screws (ZPS) 4.0 mm Cancellous Screw Fully Threaded, 12 mm Length 47484001200 4.0 mm Cancellous Sc
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Periarticular plating system, cancellous bone screw, partially threaded, hex head, 4.0 mm diameter, 16 mm length 47234
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Zimmer universal locking system (ULS) 3.5 mm cortical screw selftapping 18 mm length 47493501801
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping, 14 mm Length 47482701401
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
May 25, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping, 10 mm Length 47483501001 3.5 mm Cortical Screw Sel
Hazard: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
April 13, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 18mm Sterile For use in tot
Hazard: The firm received a customer complaint establishing that the product (Persona PS Articular Surfaces)information shown on the box differed by sides. One side showed P/N: 42-5114-008-18/ Lot: 62632101 and the other side showed P/N: 42-5114-005-14/ Lot: 62646580.
April 13, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 14mm Sterile. For use in to
Hazard: The firm received a customer complaint establishing that the product (Persona PS Articular Surfaces)information shown on the box differed by sides. One side showed P/N: 42-5114-008-18/ Lot: 62632101 and the other side showed P/N: 42-5114-005-14/ Lot: 62646580.
March 23, 2016Medical DevicesFDA
Zimmer Manufacturing B.V. recalls Product 72 consists of all product code: JDI and same usage: Item no: 805002202 ZIMTRON HEAD 12/14 0X22 MM For u
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 71 consists of all product under product code: JDI and same usage: Item no: 783401000 VERSYS PRESS FIT LD/FX
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 70 consists of all product under product code: JDI and same usage: Item no: 785701000 VERSYS HERITAGE FEM STE
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 69 consists of all product under product code: JDI and same usage: Item no: 785301701 VERSYS CEMENTED FEM STE
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 68 consists of all product under product code: JDI and same usage: Item no: 787101360 VERSYS CEM/REV/CALCAR 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 67 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTE
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 66 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTE
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 65 consists of all product under product code: KTT and same usage: Item no: 119413594 VERSA-FX II KEYLESS SHO
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 64 consists of all product under product code: JDI and same usage: Item no: 902605101 UNIPOLAR ENDO FEM HEAD
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 63 consists of all product under product code: LPH and same usage: Item no: 620004020 TRILOGY ACET SHELL 40MM
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 62 consists of all product under product code: LPH and same usage: Item no: 620003620 TRILOGY ACET SHELL 36MM
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 61 consists of all product under product code: JWH and same usage: Item no: 598003712 STD PRECOAT 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 60 consists of all product under product code: HSB and same usage: Item no: 225207055 RECON SCREW LG 5.5MM DI
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 59 consists of all product under product code: JWH and same usage: Item no: 42540000026 PSN ALL POLY PAT PLY
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 58 consists of all product under product code: HRS and same usage: Item no: 234800904 PROXIMAL DORSAL ULNA PL
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 57 consists of all product code: JDI and same usage: Item no: 763401000 PRESSFIT FEM ST FX 10 X 115 76340110
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.