Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CrossFT Punch Recalled by Linvatec Corp. dba ConMed Linvatec Due to ConMed Linvatec recalled lot number #156920, PFT-45M, CrossFT...
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
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.
Quantity: 2
Why Was This Recalled?
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.
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