FDAFDA · Food and drugs·Recall number Z-0832-2013
CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood and blood products through a needle or catheter inserted into the patient's artery or vein.
Published February 27, 2013 · Recall initiated: December 20, 2012
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 SmartSite¿ Gravity Blood Set as a result of a potential for separation at the connection of the drip chamber and tubing . The separation may be observed at priming or observed during use. If a separation between the drip chamber and tubing occurs, this could cause a delay in treatment.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Carefusion 303 Inc
- Distributor
- Nationwide Distribution including the states of AK, CA, CO, IL, MO, NV, NY, TX and UT.
- Lot
- Lot number 12055225
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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