Zimmer Anatomical Shoulder Prosthesis, Glenoid, Cemented… recallZ-1194-2007 · Zimmer Inc. · initiated Jun 25, 2007
Terminated All recalls posted in August 2007
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Zimmer Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
The package actually contains a knee patellar implant.
FDA root cause category: Other
What the company is doing
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.
Recall details
- Recall number
- Z-1194-2007
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Jun 25, 2007
- Posted by the FDA
- Aug 23, 2007
- Recalling firm
- Zimmer Inc.
- Quantity
- 10
- Product code
- KWS
- FDA submissions
- K990136
- Distribution
- Maryland.
Product description
Zimmer Anatomical Shoulder Prosthesis, Glenoid, Cemented, sterile; REF 01.04214.370.
Code information (models, lots, serial numbers)
Lot 2385941.
Other devices under the same FDA submission
1 device cleared under K990136 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Anatomical Shoulder™ Glenoid 01.04214.370Zimmer GmbH · PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED3 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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