CareFusion 303, Inc.: Medical Device Recall in 2016 - (Recall #: Z-1239-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092

Product Classification:

Class II

Date Initiated: February 12, 2016

Date Posted: March 30, 2016

Recall Number: Z-1239-2016

Event ID: 73315

Reason for Recall:

CareFusion is recalling the Alaris PC unit because a component on the PC unit power supply may cause a "System Error" or "Missing Battery" error code (120.4630).

Status: Terminated

Product Quantity: 170 units

Code Information:

Serial No. 4044845 9950535 4064411 12475162 4045659 9899143 3606478 4021398 4093501 4043745 4063430 4094994 9907675 9945292 9922622 4043375 12409069 4020663 12498854 4044531 4058193 12351849 4064030 9925068 12426138 4063830 4063911 9945269

Distribution Pattern:

Nationwide in US: AR, AZ, CA, FL, GA, IN, KY, MD, MI, MN, MO, NJ, NM, NY, OH, OR, PA, SC, TN, TX, VA, WI.

Voluntary or Mandated:

Voluntary: Firm initiated