FDA Recall Terminated

Zimmer Most Hinged Tibia Baseplate Spacer, size 1, 6 mm, sterile, Zimmer, Warsaw, IN; REF 5020-06-001. Component used to augment uni- and bi-compartmental defects and is manufactured from Ti-6A1-4V Alloy.

Recall: Z-0996-2009 · Initiated January 29, 2009

Recall

Recall Number
Z-0996-2009
Event Number
51039
Firm
Zimmer Inc.
FEI Number
1000220733
Product Code
KRO
Status
Terminated
Root Cause
Packaging process control
Initiated
January 29, 2009
Posted
March 9, 2009
Terminated
November 12, 2009
Address
345 E Main St, Warsaw, IN, 46580-2746

Description

Zimmer Most Hinged Tibia Baseplate Spacer, size 1, 6 mm, sterile, Zimmer, Warsaw, IN; REF 5020-06-001. Component used to augment uni- and bi-compartmental defects and is manufactured from Ti-6A1-4V Alloy.

Reason

The package contains 11 mm screws instead of the specified 6 mm screws.

Action

The consignee in Germany was notified by an Urgent: Device Recall letter dated 1/29/09, and delivered by email on 2/19/09. The letter stated the reason for the recall and clinical implications. The firm asked the consignee to stop using the provisional and quarantine it immediately; physically count all affected product and record data on the Inventory Return Certification Form included with letter; fax a copy of the completed form to Zimmer, Inc at 574-371-8603; request an IRA from Lindsey Arnett; and return recalled product along with completed Inventory Return Certification Form and IRA to Simmer Distribution Center. The letter states that credit will be issued upon receipt of the returned product. Also, if product has been further distributed, a copy of the recall letter should be provided to the customers. Questions or assistance should be directed to Zimmer, Inc at 1-800-613-6131.

Distribution

International Distribution only -- Country of Germany.

Quantity

3