Reported Dec 25, 2013 · Terminated
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Aesculap, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aesculap, Inc. · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
- Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
- Lot codes and dates
- lots
51468773514475885146830251503760515713945158513651447597
- lots
- Amount recalled
- 24
Where it was sold
Why it was recalled
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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