FDA Device recall Z-1303-2013
Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508
- FDA Device
- Class III
- terminated
- Published 2013-05-22
On 2013-05-22 the FDA classified a Class III recall of Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508 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-1303-2013 |
| 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 I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start 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 | Product 80530: 032887164, 203184264,110983764, 208286764, 116480564, 221590564, 120987864, 236385564,127085464; Product 8508: 207383964, 23489464 |
|---|
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-1303-2013%22
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