Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R) Recalled by Aesculap, Inc. Due to The manufacturer informed the recalling firm of a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aesculap, Inc. directly.
Affected Products
Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Quantity: 2
Why Was This 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.
Where Was This Sold?
This product was distributed to 2 states: PA, TN
About Aesculap, Inc.
Aesculap, Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report