FDAFDA · Food and drugs·Recall number Z-1459-2014
SmartSite Extension Set, Model No. 20029E, intravascular administration set.
Published April 23, 2014 · Recall initiated: March 19, 2014
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
Disconnections and leakages at the connection of the smallbore tubing and the SmartSite Y-port.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- CareFusion 303, Inc.
- Distributor
- USA Nationwide Distribution in the states of: AR, AZ, CA, CO, FL, ID, MD, MI, NC, NV, OK, OR, PA, TX, VA, WI
- Lot
- Lot No. 13085791
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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