FILE PHOTO: Signage is seen outside of FDA headquarters in White Oak, Maryland (Reuters) -The U.S. Food and Drug Administration on Monday warned healthcare providers and facilities not to use Cardinal ...

(RTTNews) - Cardinal Health Inc. has initiated a recall of around 267 million Monoject Flush Prefilled Saline Syringes (0.9% Sodium Chloride), the U.S. Food and Drug Administration announced. The ...

Just a week after issuing a notice giving its most serious rating to Cardinal Health’s recall of certain syringes, the FDA has put out a letter to healthcare providers warning that the recall may not ...

The FDA has alerted healthcare providers not to use Cardinal Health (NYSE:CAH) Monoject syringes with syringe pumps and patient-controlled analgesia, or PCA, pumps until it further evaluates reports ...

The FDA has doled out its most serious classification to a recall of some Cardinal Health medical supplies. In this case, the recall doesn’t describe a product removal, but merely a correction to the ...

Only days after MD+DI reported Cardinal Health was embroiled in a Class I recall of its Cardinal branded Monoject syringes, FDA has moved to clarify its advice for clinicians specific to the recall.

Cardinal Health is warning customers of more than 32 million syringes because they have different dimensions than older brands, resulting in compatibility issues with syringe pumps, the FDA said Nov.

Nov 20 (Reuters) - The U.S. Food and Drug Administration on Monday warned healthcare providers and facilities not to use Cardinal Health's (CAH.N), opens new tab Monoject syringes with ...