FDA-Device2012-10-24Class II
Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Aesculap, Inc.
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.
Sold states
Within the US, product was distributed to PA and TN.
Affected count
2
Manufactured in
3773 Corporate Pkwy, N/A, Center Valley, PA, United States
Products
Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0082-2013Don't want to check this manually?
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