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Recall company profile

Zimmer Manufacturing B.V. Recalls

Overview of recall records associated with Zimmer Manufacturing B.V., including dates, categories and classifications where available.

88recall records

May 25, 2016latest record date

Dec 30, 2015earliest record date

Recall history in this database

Classification mix: Class II: 88.

Medical DeviceMar 23, 2016

Zimmer Manufacturing B.V Product 11 consists of all product under product code JDI , and recall — FDA Z-1109-2016

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 33 consists of all product under product code: JDI and same recall — FDA Z-1131-2016

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 38 consists of all product under product code: HSB and same recall — FDA Z-1136-2016

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 58 consists of all product under product code: HRS and same recall — FDA Z-1156-2016

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 55 consists of all product under product code: HSB and same recall — FDA Z-1153-2016

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 6 consists of all products under product code HWC, and same recall — FDA Z-1104-2016

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 2 consists of all products product code LPH, and same recall — FDA Z-1100-2016

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 61 consists of all product under product code: JWH and same recall — FDA Z-1159-2016

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 68 consists of all product under product code: JDI and same recall — FDA Z-1166-2016

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 21 consists of all product under product code: JDI and same recall — FDA Z-1119-2016

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 23 consists of all product code: JDI and same usage: Item recall — FDA Z-1121-2016

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 44 consists of all product under product code: HWC and same recall — FDA Z-1142-2016

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 24 consists of all product under product code: HRS and same recall — FDA Z-1122-2016

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 72 consists of all product code: JDI and same usage: Item recall — FDA Z-1170-2016

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 DeviceJan 13, 2016

Zimmer Manufacturing B.V NexGEN System REF 5980-37-01 Tibial Component Size Stemmed 3 recall — FDA Z-0590-2016

A product complaint was received stating that a carton labeled as a Precoat Stemmed Tibia Size 3 was opened for use and the contents were a non-augmented Stemmed Tibia Plate size 3.

Class IIFDA: TerminatedZimmer Manufacturing B.V.

Medical DeviceDec 30, 2015

Zimmer Manufacturing B.V Label reading in part as: "NexGen System, Complete Knee Solution recall — FDA Z-0449-2016

Complaints were received from Thailand reporting that there was no white paper (Tyvek) seal on the inner package of P/N:00-5980-037-01 unit from lot #62460264

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.