FDA Device recall Z-1304-2013
Curity Staple Remover Kit
- FDA Device
- Class III
- terminated
- Published 2013-05-22
On 2013-05-22 the FDA classified a Class III recall of Curity Staple Remover Kit by Covidien, citing on March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodin….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1304-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-04-12 |
| Published | 2013-05-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Covidien |
| Distribution | US |
Product
Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit.
Reason
On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in specific convenience kits.
Identifiers
| code_info | 103387264, 117881264, 110983964, 214981164, 117488864 |
|---|
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-1304-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.