FDA Medical Device Recalls (openFDA)
Stryker Howmedica Osteonics Corp.: X-Celerate Universal Block Pegless Size #3, Non Sterile;
- Recall number
- Z-1691-2008
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Product
- X-Celerate Universal Block Pegless Size #3, Non Sterile;
- Status
- Terminated
- Initiated
- 2008-03-18
- Posted
- 2008-09-20
- Terminated
- 2010-10-25
- Reason
- Discovery of the potential for Pin and Punch interference of the Size 3 Scorpio Notch Preparation Guide that may result in damage to bone if a user aggressively attempts to seat an obstructed punch.
- Root cause
- Device Design
- Action
- Urgent Product Correction notification letters were sent via Federal Express, return receipt to all users on March 18, 2008. Questions should be directed to Rita Intorella, Divisional Regulatory Reporting at (201) 831-5825.
- Quantity
- 175 units in US, 453 units internationally
- Distribution
- Products were distributed worldwide.
- Lot, serial or model codes
- All lot codes since 1998; Catalog Number 8000-3303
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LXH
- 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