device · product 1 of 1
Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC
- Recall number
- Z-2107-2021
- Initiated
- June 14, 2021
- Classification
- Class II
- Status
- Ongoing
- Recalling firm
- Arthrex, Inc.
- Quantity
- 3985 pieces
App-derived interpretation
Not properly sterilized, because the outer pouch seal on the Tyvek header was sealed closely to the foil pouch.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Inspect official wording and provenance
Reason for recall
Not properly sterilized, because the outer pouch seal on the Tyvek header was sealed closely to the foil pouch.
Code information
Lots 12758314 and 13022357
Distribution pattern
US Nationwide Distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV and Hawaii.