FDA Medical Device Recalls (openFDA)
Stryker Howmedica Osteonics: Crossfire Acetabular II Insert. Catalog No: 2041C-2642.
- Recall number
- Z-0560-04
- Recalling firm
- Stryker Howmedica Osteonics
- Product
- Crossfire Acetabular II Insert. Catalog No: 2041C-2642.
- Status
- Terminated
- Initiated
- 2004-01-09
- Posted
- 2004-07-20
- Terminated
- 2004-03-08
- Reason
- This device is not approved for sale in the US.
- Root cause
- Other
- Action
- Letters dated 1/9/2004 and 1/12/2004 were sent to Surgical Resources and Dr. Vorenkamp alerting them to the situation.
- Quantity
- 3 (1 unit in US)
- Distribution
- The one device was shipped to Surgical Resources, 1150 Torrey Road, Suite A, Fenton, MI 48430 for Dr. Steven E. Vorenkamp, M.D., Petoskey, MI..
- Lot, serial or model codes
- Lot 48921601
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JDL
- 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