Arthrocare SPORTS MEDICINE — Class II medical device recall Z-0652-2014
Terminated recall by ArthroCare Medical Corporation, reported 2014-01-15, distributed nationwide. A sharp edge on the cannulated tip of the device may damage or cut a suture.
| Recall number | Z-0652-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ArthroCare Medical Corporation, Austin, TX, United States |
| Recall initiated | 2013-12-09 |
| Classified | 2014-01-09 |
| Reported by FDA | 2014-01-15 |
| Terminated | 2015-04-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CH, DE, ES, FR |
| Quantity | 76 |
| Lot numbers | 1049402, 2013-10 |
| Model numbers | 25-3011 |
Product
Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
Reason for recall
A sharp edge on the cannulated tip of the device may damage or cut a suture.
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-0652-2014. 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.