FDA Medical Device Recalls (openFDA)
Stryker Howmedica Osteonics: Femoral Resection Guide, Scorpio L.R.S. Instrumentation.
- Recall number
- Z-1143-03
- Recalling firm
- Stryker Howmedica Osteonics
- Product
- Femoral Resection Guide, Scorpio L.R.S. Instrumentation.
- Status
- Terminated
- Initiated
- 2003-07-17
- Posted
- 2003-08-21
- Terminated
- 2003-09-03
- Reason
- Scorpio Femoral Resection Guides have the potential to remove more bone than necessary.
- Root cause
- Other
- Action
- Product recall letters and product accountability forms were sent via FedEx to all Branches/sales agents on July 17, 2003. For the Canadian and International customers, the recall notification was also sent on July 17, 2003. All devices are to be returned to Howmedica Osteonics, Mahwah, NJ.
- Quantity
- 102
- Distribution
- The catalog numbers were sent to Howmedica Osteonics Sales Representatives/agents, one Canada Howmedica Sales Representative, and one International Howmedica location in Ireland.
- Lot, serial or model codes
- Catalog No: 8050-5103; 8050-5105; 8050-5107; 8050-5109; 8050-5111; 8050-5113.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- HTZ
- Firm FEI
- 3003070421
- Firm city
- Mahwah
- Firm state
- NJ
- 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