The affected lots include:-- 8881570121 Monoject 0.9 percent Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill 13A0084N, 13A0094, 13B0364, 13C0504, 13C0514.

The Food and Drug Administration has categorized Cardinal Health’s recall of disposable syringes as a Class I event, reflecting problems that have led to an unspecified number of injuries ...

The recall includes 12mL Syringe, 10 mL Saline Fill with SKU 8881570121; 12mL Syringe, ... Meanwhile, Monoject 3mL syringe, 2.5mL Saline Fill is not affected by the recall.

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 ...

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 ...

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 ...

Aligned Medical Solutions initiated a nationwide recall of Cardinal Health’s Monoject™ Flush Prefilled Saline Syringes placed into 9,378 kits. These convenience kits have been found to contain ...

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 patient ...