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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 ...
Covidien is recalling certain lots of Monoject prefill flush syringes due to the risk of some non-sterile fluid and mismatched tip cap, label, volume, and wrapper. Skip to navigation Skip to main ...
On Friday, the company announced a recall for the removal of all sizes of two Cardinal Health-brand Monoject syringes, and the FDA released its own notice publicizing the action. Cardinal said it ...
They’re all luer-lock tip Monoject syringes, with sizes ranging from one to 60 milliliters. Related. Baxter infusion pumps face another Class I recall, this time for possible false alarms.
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 ...
Cardinal Health primarily sells Monoject and Magellan. Monoject is a standard syringe, while Magellan is a hinged safety syringe. The hinged safety syringe market represented the largest segment of ...
The affected products include the BD Alaris Syringe Module, BD Alaris PCU, and Alaris PCA Module; model numbers: 8110, 8015, and 8120. These products were distributed between June 19, 2004 and ...
Meanwhile, Monoject 3mL syringe, 2.5mL Saline Fill is not affected by the recall. This item, SKU 8881570300, will be available for sale until inventory is depleted.
It said the dimensional changes made to Cardinal Health’s Monoject syringes, when used with syringe pumps or patient-controlled analgesia (PCA) pumps, may result in issues that include overdose ...
The FDA has alerted healthcare providers not to use Cardinal Health (CAH) Monoject syringes with syringe pumps and patient-controlled analgesia pumps over compatibility concerns.