Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
"***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC 11311 CONCEPT BLVD Recalled by Linvatec Corp. dba ConMed Linvatec Due to ConMed Linvatec is recalling the product due to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Linvatec Corp. dba ConMed Linvatec directly.
Affected Products
"***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.
Quantity: 2 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Linvatec Corp. dba ConMed Linvatec
Linvatec Corp. dba ConMed Linvatec has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report