Arthrex, Inc. recalls Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anc
See all recalls from Arthrex, Inc. →Recalled Product
Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Number AR-1317FT Product Usage: Soft tissue fixation to bone in the hand and wrist
Hazard / Issue
Potentially lead to anchor breakage during insertion,
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lots #: 10175216, 1075219, 10199557, and 10199558
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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Search Amazon for Arthrex Suture Anchor, Nano →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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