Carefusion 303 Inc: Medical Device Recall in 2013 - (Recall #: Z-0832-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: December 20, 2012

Date Posted: February 27, 2013

Recall Number: Z-0832-2013

Event ID: 64204

Reason for Recall:

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.

Status: Terminated

Product Quantity: 5,050 units

Code Information:

Lot number 12055225

Distribution Pattern:

Nationwide Distribution including the states of AK, CA, CO, IL, MO, NV, NY, TX and UT.

Voluntary or Mandated:

Voluntary: Firm initiated