Synthes Cannulated Distal Femoral Nail recall
Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile. Orthppedic implant device.
Why was Synthes Cannulated Distal Femoral Nail recalled?
Firm discovered that a nail that was within the scope of a previous Trauma Nail recall had been distributed.
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?
Part Number 450.851S, Lot Number 7065061
- Product
- Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile. Orthppedic implant device.
- Recalling firm
- Synthes USA HQ, Inc.
- Quantity
- 1
- Distribution
- US distribution to MA.
- Recall date
- September 25, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)