Stryker Howmedica Osteonics Triathlon tibial alignment recall
Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp extramedullary (EM) referencing instrument (Cat. No. 6541-2-609), for use in Total…
Why was Stryker Howmedica Osteonics Triathlon tibial alignment recalled?
Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
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 #6541-2-609 All lot codes
- Product
- Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp extramedullary (EM) referencing instrument (Cat. No. 6541-2-609), for use in Total…
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 10,537 units
- Distribution
- Nationwide Distribution
- Recall date
- September 4, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)