Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ENDOPLUS Recalled by Endoplus, Inc. Due to Multiple complaints reporting that the moveable jaw has...
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 Endoplus, Inc. directly.
Affected Products
ENDOPLUS; Precision Laparoscopic Instruments; REF 346VA; Description 5mm Atraumatic Grasper S/A, Standard; Non-sterile; Manufactured by Endoplus; 750 Tower Rd., Suite A, Mundelein, IL 60060 USA. Intended for grasping, dissecting, retraction, clamping in conjunction with the laparoscopic during laparoscopic surgery.
Quantity: 81 units
Why Was This Recalled?
Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.
Where Was This Sold?
This product was distributed to 3 states: FL, TX, VA
About Endoplus, Inc.
Endoplus, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report