Stryker Howmedica Osteonics Corp. Allocraft TLIF Bone Inserter. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Allocraft TLIF Bone Inserter.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog No. 483600100, Lot Code: 04C570
Products Sold
Catalog No. 483600100; Lot Code: 04C570
Stryker Howmedica Osteonics Corp. is recalling Allocraft TLIF Bone Inserter. due to Stryker was made aware that the short arm of the bone inserter may fracture during use and potentially result in an adverse health consequence.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Stryker was made aware that the short arm of the bone inserter may fracture during use and potentially result in an adverse health consequence.
Recommended Action
Per FDA guidance
The firm sent notification letters to their branches/agencies on 4/4/2005. 100% effectiveness to be achieved by completing Product Accountability forms, follow up telephone calls, and follow-up letters as required.
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