Zimmer Manufacturing B.V. Recalls — U.S. Recall Records

Recall history in this database

Classification mix: Class II: 88.

Medical DeviceMay 25, 2016

Zimmer Manufacturing B.V VersaFx Femoral Fixation System Hex head compression screw 4.7 mm recall — FDA Z-1682-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Manufacturing B.V ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter recall — FDA Z-1681-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Manufacturing B.V Trilogy self-tapping bone screw Bone screw 4.5x25 selftap recall — FDA Z-1684-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Manufacturing B.V M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm recall — FDA Z-1678-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Plates and Screws (ZPS) 4.0 mm Cancellous Screw Fully Threaded, 12 mm Length recall — FDA Z-1677-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer universal locking system (ULS) 3.5 mm cortical screw selftapping 18 mm length recall — FDA Z-1675-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Manufacturing B.V Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp recall — FDA Z-1683-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping, 14 mm Length 47482701401 recall — FDA Z-1674-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Manufacturing B.V Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 45 recall — FDA Z-1680-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping, 10 mm Length 47483501001 recall — FDA Z-1673-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Manufacturing B.V Mini MagnaFx Cannulated Screw Fixation System Small Cannulated Bone recall — FDA Z-1679-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMay 25, 2016

Zimmer Manufacturing B.V Periarticular plating system, cancellous bone screw, partially recall — FDA Z-1676-2016

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceApr 13, 2016

Zimmer Manufacturing B.V Persona The Personalized Knee System Articular Surface Posterior recall — FDA Z-1340-2016

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:…

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceApr 13, 2016

Zimmer Manufacturing B.V Persona The Personalized Knee System Articular Surface Posterior recall — FDA Z-1341-2016

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:…

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 25 consists of all product under product code: LPH and same recall — FDA Z-1123-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 48 consists of all product under product code: JWH and same recall — FDA Z-1146-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 12 consists of all product under product code JDI , and recall — FDA Z-1110-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 31 consists of all product under product code: KTT and same recall — FDA Z-1129-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 29 consists of all product under product code: LPHand same recall — FDA Z-1127-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 52 consists of product code: HWC and same usage: Item no recall — FDA Z-1150-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 18 consists of all product under product code: HWC and same recall — FDA Z-1116-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 5 consists of all products under product code HWC, and same recall — FDA Z-1103-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 28 consists of all product under product code: JDI and same recall — FDA Z-1126-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 51 consists of all product under product code: JWH and same recall — FDA Z-1149-2016

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.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Understanding this recall history

This page summarizes recall records in which the official source identifies Zimmer Manufacturing B.V. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.