Integra LifeSciences Corp.: Medical Device Recall in 2019 - (Recall #: Z-2435-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Integra Jarit GEMINI CLAMP 9 1/4 inch - used in vascular and cardiothoracic procedures used for clamping and occluding vessels. Cat. #140-332

Product Classification:

Class II

Date Initiated: August 7, 2019

Date Posted: September 11, 2019

Recall Number: Z-2435-2019

Event ID: 83418

Reason for Recall:

A small crack at the box lock corner may after multiple cleaning and sterilization cycles produce an increased risk of corrosion, weakening the instrument and resulting in premature need for replacement and/or breakage of the instrument

Status: Terminated

Product Quantity: 237 units

Code Information:

Lot #AA1901

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated