FDAClass IISeptember 7, 2016

The 9025TRU Arterial Blood Gas recall

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

Why was The 9025TRU Arterial Blood Gas recalled?

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.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis.
Recalling firm
Cardinal Health
Quantity
Lot #884993 -16,000 units, Lot #903136 -1,900 units and Lot #903137 - 300 units.
Distribution
Worldwide Distribution - US (nationwide) and Canada.
Recall date
September 7, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls