Hospira Carpuject Recall Issued Due to Potential Leaks of Some Drug Products
Failure of the Carpuject injection seals may lead to the need for further medical treatment, the FDA warns.
Tag Archives: Syringe Recall
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Sol-Millennium Syringe Recall Issued Amid FDA Crackdown on Plastic Chinese-Made Syringes
Recalled Chinese syringes were not approved by the FDA, and may be prone to leaking and breaking, causing life-threatening injuries and complications
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Cardinal Health Gets Warning Letter Over Defective Monoject Syringes
FDA never approved recent changes in manufacturers and new dimensions for the syringe sizes, which led to a massive Monoject syringe recall earlier this year
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Cardinal Health Monoject Recall Expanded to Impact Nearly 28M Syringes
The FDA has declared a February product correction as a Class I Monoject syringe recall, following numerous reports of problems with the new syringes' dimensions.
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Cardinal Health Monoject Syringe Recall Issued Over Problems Fitting Drug Pumps
The FDA first warned of problems with Cardinal Health Monoject syringes failing to fit drug pumps in November 2023.
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BD Alaris Infusion Pump Recall Linked to Problems with Monoject Syringes
About a dozen incompatibility problems with Alaris infusion pumps and Cardinal Health Monoject syringes have been reported.
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FDA Warns “Do Not Use” Cardinal Health Monoject Syringes With Syringe Pumps and PCA Pumps
Warning comes after Cardinal Health recalled more than 32 million syringes in September, because they may not fit correctly into certain pain management drug pumps.
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Fresenius Sanxin Single Use Syringe Recall Issued Due to Risk of Blood, Heparin Leaks
The FDA warns that the recalled syringes could cause infections, blood loss, increased blood clot risks, embolism and death.
