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ConMed Corporation recalls Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be use
Recalled December 20, 2017 · FDA recall Z-0253-2018 · ConMed
Hazard
Manufactured with the incorrect anchor outer body · FDA Class II
Units
56 units
Sold at
CA, IN, KS, MD, NY, OH, PA, TN, TX & WI
Description
Manufactured with the incorrect anchor outer body
Product
Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be used in either arthroscopic or open surgical procedures.
Manufacturer(s)
ConMed Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →