Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Reported: December 25, 2013 Initiated: September 19, 2013 #Z-0492-2014
Product Description
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Reason for Recall
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
Details
- Recalling Firm
- Aesculap, Inc.
- Units Affected
- 24
- Distribution
- Distributed in FL and MD.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7. Recalled by Aesculap, Inc.. Units affected: 24.
Why was this product recalled? ▼
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 25, 2013. Severity: Moderate. Recall number: Z-0492-2014.
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