Cardinal Health: Medical Device Recall in 2016 - (Recall #: Z-2713-2016)

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:

The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis.

Product Classification:

Class II

Date Initiated: June 27, 2016

Date Posted: September 7, 2016

Recall Number: Z-2713-2016

Event ID: 74706

Reason for Recall:

Arterial Blood Gas (ABG) Kit- Missing Safety Component. The ABG Kit(s) have been identified as missing the locking clasp component. CareFusion/BD has identified a potential customer/user safety risk associated with the missing locking clasp component.

Status: Terminated

Product Quantity: Lot #884993 -16,000 units, Lot #903136 -1,900 units and Lot #903137 - 300 units.

Code Information:

Three (3) total lots (lot #884993, lot #903136 & lot #903137).

Distribution Pattern:

Worldwide Distribution - US (nationwide) and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated