Cardinal Health, Inc.

Location

Ohio

Founded

1979-02-28

Risk Signals

3280 news mentions monitored

Industry Context

This company is tracked across risk categories, including those related to its sector (e.g., Medical, Dental, and Hospital Equipment and Supplies, Drugs, Drug Proprietaries, and Druggists' Sundries, Management Services), including supply chain integrity, ESG practices, labor disputes, and regulatory compliance.

Recent Articles about Cardinal Health, Inc.

Live alerts from global media, monitored by Business Radar

FDA Lists 27 Eye Drop Products that May Cause Infections

2024-06-13 (health.com)

FDA Lists 27 Eye Drop Products that May Cause Infections

The FDA is asking consumers to stop using 27 eye drop products over concerns that they're not sterile, and could cause eye infections as a result. CVS Health, Walmart, Target, and other brands were included on in FDA's warning, and one company, Leader (Cardinal Health) has since issued a recall.

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FDA broadens warnings over recalled Cardinal Health syringes

2024-03-03 (fiercebiotech.com)

FDA broadens warnings over recalled Cardinal Health syringes

After giving its most serious rating to Cardinal Health’s syringe recall, the FDA warned healthcare providers that the recall may not go far enough.

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Becton Dickinson (BD)/Carefusion 303 Recalls Alaris Infusion Pumps Due to Compatibility Issues with Cardinal Health Monoject Syringes

2023-12-19 (fda.gov)

Becton Dickinson (BD)/Carefusion 303 Recalls Alaris Infusion Pumps Due to Compatibility Issues with Cardinal Health Monoject Syringes

BD/Carefusion 303 is recalling their Alaris Infusion Pumps to make a correction on compatibility issues with Cardinal Health Monoject syringes.

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Compatibility Issues Prompt Recall of Alaris Infusion Pumps

2023-12-11 (endocrinologyadvisor.com)

Compatibility Issues Prompt Recall of Alaris Infusion Pumps

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.

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Who can qualify for the 2023 eye drop recall lawsuits

2023-12-09 (islandernews.com)

Who can qualify for the 2023 eye drop recall lawsuits

In October, the Food and Drug Administration (FDA) released an updated list of over-the-counter artificial tears products that consumers should not purchase or use.

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Compatibility Issues Prompt Recall of Alaris Infusion Pumps

2023-12-06 (empr.com)

Compatibility Issues Prompt Recall of Alaris Infusion Pumps

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.

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Becton Dickinson Infusion Pump Recalled for Compatibility Issue

2023-12-04 (24x7mag.com)

Becton Dickinson Infusion Pump Recalled for Compatibility Issue

Becton Dickinson is recalling their Alaris Infusion Pumps due to compatibility issues with Cardinal Health Monoject syringes.

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Health News Roundup: AstraZeneca calls off two late-stage potassium drug trials; US FDA gives second approval to Eli Lilly's drug for type of blood cancer and more | Health

2023-12-03 (devdiscourse.com)

Health News Roundup: AstraZeneca calls off two late-stage potassium drug trials; US FDA gives second approval to Eli Lilly's drug for type of blood cancer and more | Health

The Danish drugmaker is working to convince European governments and insurers to reimburse the drug, seeking to position it as more than a lifestyle drug. EU watchdog seeks more data from GLP-1 drugmakers on suicidal thoughts The EU 's drug watchdog will request more data from makers of a class of

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FDA warns against using Cardinal’s syringes

2023-11-20 (wsau.com)

FDA warns against using Cardinal’s syringes

(Reuters) -The U.S. Food and Drug Administration on Monday warned healthcare providers and facilities not to use Cardinal Health's Monoject syringes w...

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FDA announces recall of more than 32 million disposable syringes

2023-11-14 (healthexec.com)

FDA announces recall of more than 32 million disposable syringes

The new-look syringes are causing significant issues when used with syringe infusion pumps. This is a Class I recall, which means the FDA believes the products “may cause serious injuries or death.”

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BEWARE! Here Is Every Store That Eye Drops and Gels Are Being Recalled In Texas

2023-11-13 (ktemnews.com)

BEWARE! Here Is Every Store That Eye Drops and Gels Are Being Recalled In Texas

Eye drops and gels have been recalled in Texas at these stores.

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Nurse Assist Recalls Sodium Chloride Irrigation, Sterile Water

2023-11-07 (rttnews.com)

Nurse Assist Recalls Sodium Chloride Irrigation, Sterile Water

Nurse Assist, LLC is recalling 0.9% sodium chloride irrigation USP and sterile water for irrigation USP citing the potential for a lack of sterility assurance, the U.

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