Trident Insert Impactor
This recall has been terminated (originally issued May 29, 2003).
- Company
- Stryker Howmedica Osteonics
- Recall Initiated
- April 28, 2003
- Posted
- May 29, 2003
- Terminated
- November 12, 2003
- Recall Number
- Z-0901-03
- Quantity
- 1758
- Firm Location
- Mahwah, NJ
- Official Source
- View on FDA website ↗
Reason for Recall
The ball retaining sleeve on the Trident Insert Impactor can possibly disassemble.
Distribution
The product has been distributed the Howmedica branches and sales reps, hospitals, and International Howmedica distributors located in Sweden, China, France, Netherlands, Germany, Spain, Australia, Japan, New Zealand, Switzerland, Portugal, England, Chile, and Brazil.
Lot / Code Info
Catalog Number: 2111-0000
Root Cause
Other
Action Taken
Howmedica sent recall letters and acknowledgement forms via FedEx on April 29, 2003 with return receipt.
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