Aju Pharm Co., Ltd. recalls Genesis Push-In Suture Anchor
Recalled Product
Genesis Push-In Suture Anchor
Hazard / Issue
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Model No. 10S30002; All UDI Codes; All Lots.
View official government recall
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