FDAFDA · Food and drugs·Recall number Z-0406-2014
Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended for fractures, osteotomies, and replantations of small bones including the foot, ankle, and hand.
Published December 4, 2013 · Recall initiated: July 30, 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
A complaint was reported regarding a screw being found in a package labeled for 2.4 mm LC-DCP Plate.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Synthes (USA) Products LLC
- Distributor
- Worldwide Distribution - USA (nationwide) including IN, NY, WA, NE, MD, TX, AL, MI, and Internationally to Canada.
- Lot
- Part No. 249.926, lot No. 8093100
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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