Recall Z-0652-2014— ArthroCare Medical Corporation
Class II · Terminated
Class II FDA medical device recall by ArthroCare Medical Corporation, initiated 2013-12-09, terminated 2015-04-08. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- ArthroCare Medical Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-12-09
- Terminated
- 2015-04-08
- Firm location
- Austin, TX, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.