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Aesculap, Inc. recalls Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Recalled October 24, 2012 · FDA recall Z-0082-2013 · Aesculap
Hazard
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. · FDA Class II
Units
2
Sold at
Within the US, product was distributed to PA and TN.
Description
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.
Product
Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Manufacturer(s)
Aesculap, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →