Linvatec Corp. dba ConMed Linvatec: Medical Device Recall in 2012 - (Recall #: Z-2147-2012)

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:

CrossFT Punch, Product Number PFT-45M. Manufacturer: CONMED LINVATEC. The intended use is to create a hole to facilitate insertion of the CrossFT suture anchor into bone.

Product Classification:

Class II

Date Initiated: August 12, 2011

Date Posted: August 15, 2012

Recall Number: Z-2147-2012

Event ID: 62395

Reason for Recall:

ConMed Linvatec recalled lot number #156920, PFT-45M, CrossFT Punch because there is a possibility that the device was etched incorrectly listing the item number as PFT-00M and includes incorrect depth lines for insertion.

Status: Terminated

Product Quantity: 2

Code Information:

Lot #156920

Distribution Pattern:

Nationwide Distribution, including the states of Colorado and Pennsylvania.

Voluntary or Mandated:

Voluntary: Firm initiated