Stryker Howmedica Osteonics Corp. X-Celerate Universal Block Pegless Size #3, Non Sterile; Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
X-Celerate Universal Block Pegless Size #3, Non Sterile;
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
All lot codes since 1998, Catalog Number 8000-3303
Products Sold
All lot codes since 1998; Catalog Number 8000-3303
Stryker Howmedica Osteonics Corp. is recalling X-Celerate Universal Block Pegless Size #3, Non Sterile; due to 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 ag. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026