FDAFDA · Food and drugs·Recall number Z-0492-2014
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Published December 25, 2013 · Recall initiated: September 19, 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
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Aesculap, Inc.
- Distributor
- Distributed in FL and MD.
- Lot
- lots: 51468773, 51447588, 51468302, 51503760, 51571394, 51585136, 51447597
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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