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Linvatec Corp. dba ConMed Linvatec recalls GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only STERILE EO CONMED LINV
Recalled July 10, 2013 · FDA recall Z-1619-2013 · Linvatec Corp.
Hazard
Incorrect blue/white suture was used. · FDA Class II
Units
60 each of both units
Sold at
US Distribution including the states of FL, KY, LA, MI, NC, and NY.
Description
Incorrect blue/white suture was used.
Product
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
Manufacturer(s)
Linvatec Corp. dba ConMed Linvatec
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →