Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US) Recalled by Aesculap, Inc. Due to The trial insertion instrument may disassemble during use...
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 Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
Quantity: 30
Why Was This Recalled?
The trial insertion instrument may disassemble during use due to a potentially weak weld on then trial inserter shaft block area located near the thumb wheel.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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