Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Recalled by Linvatec Corp. dba ConMed Linvatec Due to Incorrect blue/white suture was used.
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
GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only STERILE EO CONMED LINVATEC REF CFBC-4502. Reattachment of soft tissue to bone in orthopedic surgical procedures
Quantity: 60 each of both units
Why Was This Recalled?
Incorrect blue/white suture was used.
Where Was This Sold?
This product was distributed to 6 states: FL, KY, LA, MI, NY, NC
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