FDA Medical Device Recalls (openFDA)
Zimmer Inc.: Zimmer Trabecular Metal Reverse Shoulder System Glenosphere, 40 mm diameter; Catalog/Ref No. 00-4349-040-01.
- Recall number
- Z-1417-06
- Recalling firm
- Zimmer Inc.
- Product
- Zimmer Trabecular Metal Reverse Shoulder System Glenosphere, 40 mm diameter; Catalog/Ref No. 00-4349-040-01.
- Status
- Terminated
- Initiated
- 2006-07-20
- Posted
- 2006-08-26
- Terminated
- 2007-12-19
- Reason
- Components may not lock together as intended.
- Root cause
- Other
- Action
- Consignees were notified via recall letter dated 7/20/06 to cease use of the products and to return the product to Zimmer.
- Quantity
- 197 for all three recalls Z-1416-1418-06
- Distribution
- Worldwide distribution --- USA and countries of Australia and China
- Lot, serial or model codes
- All lots.
- 510(k) numbers
- ["K052906"]
- PMA numbers
- not on file
- Product code
- KWT
- 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