FDAFDA · Food and drugs·Recall number Z-2243-2013
Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile. Orthppedic implant device.
Published September 25, 2013 · Recall initiated: April 18, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Firm discovered that a nail that was within the scope of a previous Trauma Nail recall had been distributed.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Synthes USA HQ, Inc.
- Distributor
- US distribution to MA.
- Lot
- Part Number 450.851S, Lot Number 7065061
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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