Stryker Howmedica Osteonics Trident Insert Impactor Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Trident Insert Impactor
Brand
Stryker Howmedica Osteonics
Lot Codes / Batch Numbers
Catalog Number: 2111-0000
Products Sold
Catalog Number: 2111-0000
Stryker Howmedica Osteonics is recalling Trident Insert Impactor due to The ball retaining sleeve on the Trident Insert Impactor can possibly disassemble.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The ball retaining sleeve on the Trident Insert Impactor can possibly disassemble.
Recommended Action
Per FDA guidance
Howmedica sent recall letters and acknowledgement forms via FedEx on April 29, 2003 with return receipt.
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 noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026