Arthrex, Inc. recalls Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, C
See all recalls from Arthrex, Inc. →Recalled Product
Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC
Hazard / Issue
Not properly sterilized, because the outer pouch seal on the Tyvek header was sealed closely to the foil pouch.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lots 12758314 and 13022357
✅ 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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