FDA Device recall Z-0652-2014
Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
- FDA Device
- Class II
- terminated
- Published 2014-01-15
On 2014-01-15 the FDA classified a Class II recall of Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only by Arthrocare Medical, citing A sharp edge on the cannulated tip of the device may damage or cut a suture.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0652-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-09 |
| Published | 2014-01-15 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Arthrocare Medical |
| Distribution | US |
Product
Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
Reason
A sharp edge on the cannulated tip of the device may damage or cut a suture.
Identifiers
| code_info | Catalog #25-3011, Lot #1049402 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0652-2014%22
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