Nonabsorbable suture anchor system intended to reattach soft tissue… — Class II medical device recall Z-0253-2018
Terminated recall by ConMed Corporation, reported 2017-12-20, distributed in CA, IN, KS, MD, NY, OH, PA, TN…. Manufactured with the incorrect anchor outer body
| Recall number | Z-0253-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ConMed Corporation, Utica, NY, United States |
| Recall initiated | 2017-04-17 |
| Classified | 2017-12-14 |
| Reported by FDA | 2017-12-20 |
| Terminated | 2021-08-31 |
| Distributed | CA, IN, KS, MD, NY, OH, PA, TN, TX, WI |
| Quantity | 56 units |
| Lot numbers | 786351 |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0253-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.