Reported May 22, 2013 · Terminated
Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start Kit.
Covidien LLC
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Covidien LLC · 15 Hampshire Street · Mansfield, MA · 02048-1113
Is this the product you have?
- Curity I.V. Start Kit
- Product ID80530 and Curity I.V
- Start Kit Product ID8508. IV Start Kit
- Lot codes and dates
- Product 80530
032887164203184264110983764208286764116480564221590564120987864236385564127085464
- Product 8508
20738396423489464
- Product 80530
- Amount recalled
- 17740 kits
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
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.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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