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FDAFDA · Food and drugs·Recall number Z-1303-2013

Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start Kit.

Published May 22, 2013 · Recall initiated: April 12, 2013

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Covidien LLC
Distributor
Worldwide distribution: USA (nationwide) and in the country of: Panama.
Lot
Product 80530: 032887164, 203184264,110983764, 208286764, 116480564, 221590564, 120987864, 236385564,127085464; Product 8508: 207383964, 23489464
Risk classification
Class III
Area (FDA)
device
Country
United States

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