Femoral Nail recall
Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System is one of the first femoral nailing systems to offer an option for either an antegrade…
Why was Femoral Nail recalled?
Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field.
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 number 18251032S and Lot Code K288335
- Product
- Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System is one of the first femoral nailing systems to offer an option for either an antegrade…
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 1 unit in total
- Distribution
- US distribution to state of: CA.
- Recall date
- September 21, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)