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Terminated

Zimmer Anatomical Shoulder Prosthesis, Glenoid, Cemented, sterile; REF 01.04214.370.

FDA Recall Z-1194-2007 · Posted 2007-08-23

Recalling FirmZimmer Inc.
Recall StatusTerminated
Product CodeKWS
Date Initiated2007-06-25
Date Terminated2007-12-05
Product Quantity10

Reason for Recall

The package actually contains a knee patellar implant.

Firm Action

The firm notifed the distributor via letter dated 6/25/07, and sent by email, to retrieve the product from their customers and to return the product.

Root Cause

Other

Distribution Pattern

Maryland.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K990136ANATOMICA GLENOID COMPONENTSulzer Orthopedics, Inc. · 1999-03-01

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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