Drug recall
Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
FDA recall event 67087 · Class II · ArthroCare Medical Corporation
Key facts
| Event ID | 67087 |
|---|---|
| Recall numbers | Z-0652-2014 |
| Recalling firm | ArthroCare Medical Corporation |
| Product type | Devices |
| Products | Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A sharp edge on the cannulated tip of the device may damage or cut a suture. |
| Initiation date | Dec 9, 2013 |
| Report date | Jan 15, 2014 |
| Termination date | Apr 8, 2015 |
| City | Austin |
| State | TX |
| Country | United States |
| FEI number | 3006524618 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: