FDAFDA · Food and drugs·Recall number Z-0401-2014
Synthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER Synthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER is used for buttressing multi fragmentary diatal femur fractures including: supra-condylar, intra-articular and extra articular condylar fractures, periprosthetic fractures, fractures in normal or osteopenic bone, nonunions and malunions.
Published December 4, 2013 · Recall initiated: May 29, 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 plate was inadvertently released to a sales consultant that was restricted for sale.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Synthes USA HQ, Inc.
- Distributor
- US Distribution in Colorado.
- Lot
- part 04.124.406S, lot 3771678.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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