CareFusion 303, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2700-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Alaris Pump Module model 8100

Product Classification:

Class II

Date Initiated: June 12, 2017

Date Posted: July 19, 2017

Recall Number: Z-2700-2017

Event ID: 77279

Reason for Recall:

There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.

Status: Terminated

Product Quantity: 35,940 units

Code Information:

Notification will be distributed to all Alaris Pumps customers with pumps manufactured between June 2002 through June 2004.

Distribution Pattern:

US and Canada

Voluntary or Mandated:

Voluntary: Firm initiated