Linvatec Corp. dba ConMed Linvatec: Medical Device Recall in 2012 - (Recall #: Z-0164-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

"***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA***" To create pathway for insertion of CrossFT Suture Anchor into bone.

Product Classification:

Class II

Date Initiated: April 9, 2012

Date Posted: November 7, 2012

Recall Number: Z-0164-2013

Event ID: 63090

Reason for Recall:

ConMed Linvatec is recalling the product due to the punch being mis-assembled with the incorrect handled. The correct handle is a clear anodized silver colored handle.

Status: Terminated

Product Quantity: 2 units

Code Information:

Lot # 330889 and Catalog: PFT-00M - No Expiration date

Distribution Pattern:

Worldwide Distribution--US (nationwide) including state of Minnesota and the country of Thailand

Voluntary or Mandated:

Voluntary: Firm initiated