Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
UNITRAC Pneumatic Retraction Arm. A support arm used to hold Recalled by Aesculap, Inc. Due to Changes were implemented to the UNITRAC instructions for...
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
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.
Quantity: 217
Why Was This Recalled?
Changes were implemented to the UNITRAC instructions for use to ensure safe use and potentially extend the life of the product. This included recommending the use of Sterile Cover JG901 and new Quick Release Coupling RT02OR to eliminate the need to sterilize the UNITRAC and a functional check was added prior to use to ensure optimal functionality of the UNITRAC system.
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