FDA Medical Device Recalls (openFDA)
Zimmer Inc.: Zimmer Anatomical Shoulder Prosthesis, Glenoid, Cemented, sterile; REF 01.04214.370.
- Recall number
- Z-1194-2007
- Recalling firm
- Zimmer Inc.
- Product
- Zimmer Anatomical Shoulder Prosthesis, Glenoid, Cemented, sterile; REF 01.04214.370.
- Status
- Terminated
- Initiated
- 2007-06-25
- Posted
- 2007-08-23
- Terminated
- 2007-12-05
- Reason
- The package actually contains a knee patellar implant.
- Root cause
- Other
- 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.
- Quantity
- 10
- Distribution
- Maryland.
- Lot, serial or model codes
- Lot 2385941.
- 510(k) numbers
- ["K990136"]
- PMA numbers
- not on file
- Product code
- KWS
- Firm FEI
- 1000220733
- Firm city
- Warsaw
- Firm state
- IN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28