Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0164-2013 — "All in one CrossFTPunchPFT-00M4.5mm to 6.5mmCONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA" To create pathway for insertion of CrossFT Suture Anchor into bone.

U.S. FDA — Device Enforcement · United States · 2012-04-09 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0164-2013
Date of alert: 2012-04-09
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Linvatec Corp. dba ConMed Linvatec
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0164-2013 — "***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.

Related

Recall Z-0164-2013 — "All in one CrossFTPunchPFT-00M4.5mm to 6.5mmCONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA" To create pathway for insertion of CrossFT Suture Anchor into bone.