FDA recently published a statement categorizing the recall of Cardinal Health Monoject single use Luer Lock Syringes (1, 6, 12, 20, 35, and 60mL) as Class I. The Monoject disposable syringes are used ...

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 U.S. Food and Drug Administration has warned health care giant Cardinal Health over sales of imported plastic syringes made by Jiangsu Shenli Medical Production Co. Ltd. that don't meet device ...

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.

As the FDA investigates China-made plastic syringes because of compatibility issues with syringe pumps, Cardinal Health said 32 million of its syringes are experiencing the same issue. New dimensions ...

To data, there have been 13 reported injuries. Becton Dickinson (BD)/Carefusion 303 is recalling the Alaris infusion pump due to incompatibility issues with Cardinal Health Monoject syringes. The Food ...

Months after the FDA warned clinicians about plastic syringes made in China, the agency listed violations it discovered at Cardinal Health related to the marketing of unapproved and adulterated ...

The FDA is advising U.S. healthcare providers and patients to stop using any plastic syringes in their inventories that were made in China, if possible, as it looks into a spate of quality complaints.

The U.S. FDA has followed up on reports of problematic syringes made by several companies in mainland China, recommending that U.S. suppliers, consumers and health care organizations stop using these ...

The U.S. Food and Drug Administration (FDA) on Thursday said it was assessing plastic syringes made in China for potential device failures such as leaks or breakages. The FDA added that it was aware ...