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Recall Observatory FDA recall evidence

Device product

ENDOPLUS; Precision Laparoscopic Instruments; REF 345VA; Description 5 mm Traumatic 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.

Z-2265-2013

July 15, 2013

Class II

Product summary

Firm
Endoplus, Inc.
Event
Event 66063
Status
Terminated
Classification
Class II
Quantity
9 units
Official record key
device-enforcement:Z-2265-2013

Official wording

Reason: Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.

Code information: Item: 345VA; Lot Number: F3

Distribution pattern: Distributed in the states of FL, TX, and VA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.