In mid-September, Cardinal told customers that the conical tip of its Monoject 1 mL syringe is incompatible with certain needleless IV connectors. The FDA treated that notice as a Class II recall.

Cardinal Health’s CAH Monoject syringes get unfavorable FDA recommendation following reports of delay in therapy as well as inaccurate therapy (overdose or underdose) when used with a syringe ...

The issue first came to light last September, when Cardinal Health, Inc. sent a letter to healthcare providers and consumers warning that their Monoject U-100 1 mL Insulin Syringe Luer-Lock with ...

To date, the recall includes 1-, 6-, 12-, 20-, 35- and 60-mL sizes of Cardinal-branded, luer-lock tip Monoject syringes. The company also sells 10- and 140-mL versions of its standard syringes ...

In an April 24 letter to Cardinal Health CEO Steve Mason, the FDA said the company changed from manufacturing its monoject Luer-lock tip syringes and monoject enteral feeding syringes to hiring a ...

When using the newly branded Cardinal Health Monoject syringes, the pump may refuse to operate or incorrectly estimate the volume of liquid in the syringe.

The U.S. Food and Drug Administration on Monday warned healthcare providers and facilities not to use Cardinal Health's Monoject syringes with patient-controlled pain management pumps and syringe ...

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.

The U.S. Food and Drug Administration (FDA) said on Friday that Becton Dickinson is recalling its Alaris infusion pumps due to compatibility issues with Cardinal Health's Monoject syringes.

The FDA has doled out its most serious classification to a recall of some 32 million of Cardinal Health's medical supplies.