Reported Oct 24, 2012 · Terminated
Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
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?
- Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
- Lot codes and dates
- NQ083R
- Amount recalled
- 2
Where it was sold
Why it was recalled
The manufacturer informed the recalling firm of a potential laser marking error in size identification on two Columbus 4-IN-1 Femoral Cutting Guide Instruments. The guides are correctly dimensioned, but the laser markings have been incorrectly etched.
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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