PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: December 20, 2017 Initiated: April 17, 2017 #Z-0253-2018

Product Description

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.

Reason for Recall

Manufactured with the incorrect anchor outer body

Details

Recalling Firm
ConMed Corporation
Units Affected
56 units
Distribution
CA, IN, KS, MD, NY, OH, PA, TN, TX & WI
Location
Utica, NY

Frequently Asked Questions

What product was recalled?
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.. Recalled by ConMed Corporation. Units affected: 56 units.
Why was this product recalled?
Manufactured with the incorrect anchor outer body
Which agency issued this recall?
This recall was issued by the FDA Devices on December 20, 2017. Severity: Moderate. Recall number: Z-0253-2018.