CareFusion 303, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1464-2017)

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:

MaxGuard Extension Set with Injection Site and 0.2 micron filter, Model No. ME3305

Product Classification:

Class II

Date Initiated: February 20, 2017

Date Posted: March 22, 2017

Recall Number: Z-1464-2017

Event ID: 76439

Reason for Recall:

CareFusion is recalling the MaxGuard Extension Set with Injection Site and 0.2 micron filter because of reports of separation and/or leakages between the Y-connector and tubing.

Status: Terminated

Product Quantity: 1,200 units

Code Information:

Lot No. 16016790

Distribution Pattern:

US Distribution including MA and MD

Voluntary or Mandated:

Voluntary: Firm initiated