FDAFDA · Food and drugs·Recall number Z-0435-2014
VersaSafe Extension Set, Model No. 21000M-007
Published December 11, 2013 · Recall initiated: November 8, 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
CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- CareFusion 303, Inc.
- Distributor
- Nationwide Distribution.
- Lot
- Lot No. 13066550
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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