Teleflex Medical: Medical Device Recall in 2016 - (Recall #: Z-0058-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park, NC 27709 The Percutaneous Surgical System with 5 mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the human abdomen and used to grasp, hold and manipulate tissue during laparoscopic surgery.

Product Classification:

Class II

Date Initiated: September 9, 2016

Date Posted: October 19, 2016

Recall Number: Z-0058-2017

Event ID: 75130

Reason for Recall:

The product is being recalled due to a labeling error. The Gripper Graspers are labeled as Johans Graspers and the Johans Graspers are labeled as Gripper Graspers.

Status: Terminated

Product Quantity: 160 ea. in total

Code Information:

Lot Number 73M1500175

Distribution Pattern:

US Distribution to states of: AZ, CA, FL, NY, NC, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated