Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers Recalled by Aesculap, Inc. Due to The Columbus Revision CoCr 15 mm distal and...
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
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Quantity: 24
Why Was This Recalled?
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
Where Was This Sold?
This product was distributed to 2 states: FL, MD
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