Stryker Orthopaedics Triathlon Tritanium Patella recall
Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella Inserter is part of the…
Why was Stryker Orthopaedics Triathlon Tritanium Patella recalled?
Tritanium Patella Inserter Instrument fracture during implantation. .
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Catalog No. 6541-3-530. Lot Codes: CTD2778 and CTD2779.
- Product
- Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella Inserter is part of the…
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 22 Units
- Distribution
- US Nationwide Distribution - in the states of Arizona, Florida, Kentucky, Louisiana and New Jersey.
- Recall date
- July 9, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)