Product Recalls

Warning: This Nasal Spray is NOT FDA Approved

The FDA has issued a firm warning to Salvacion USA Inc. after discovering that the company is illegally selling and distributing unapproved drugs to the...

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Urgent FDA Recall of Infant Vitamin Supplement

The FDA and manufacturer Nordic Naturals have announced a recall of approximately 3,800 bottles of infant Vitamin D3 liquid supplements. A manufacturing error has resulted...

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Another Recall of Male Enhancement Capsules Announced

Manufacturer, Today the World, announced another voluntary recall of their products due to the presence of unapproved drugs within the capsules. The supplements, marketed for...

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Nationwide Recall of Male Enhancement Capsules Announced

In cooperation with the FDA, manufacturer Today the World announced a voluntary recall of all lots of their Arize herbal dietary supplement capsules. The capsules...

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Recall of Ting® Athlete’s Foot Spray

Insight Pharmaceuticals, in cooperation with the FDA, is recalling two lots of the popular, Ting® Athlete’s Foot Spray. Independent researchers discovered dangerous levels of Benzene,...

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Nationwide FDA Recall…Children at Risk of Self-Harm

The FDA has announced a total recall of all lots of Neptune’s Fix, a series of over-the-counter substances marketed to improve brain function and treat...

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Recall: Children’s ADHD/Adult Narcolepsy Medication Mix-up

The FDA has issued a very concerning and immediate recall of a medication used to treat ADHD (attention-deficit/hyperactivity disorder) in children and Narcolepsy in adults....

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Urgent Robitussin Recall

Drug manufacturer Haleon, in cooperation with the FDA, issued an immediate, voluntary recall for eight lots of Robitussin. Inspectors found microbial contamination in the product...

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Recall Amendment Issued for Eye Drops

Due to their release of inaccurate information, Kilitch Healthcare India Limited has issued a nationwide press release providing the corrected information. Consumers who utilize the...

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FDA Adds Black Box Warning to Prolia (denosumab)

  The FDA has announced the addition of a black box warning to Prolia (denosumab), a drug often prescribed for osteoporosis. The warning is to...

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Massive Recall of IV Drugs

The FDA has announced a massive recall of several IV medications due to the possibility that they contain twice the listed dosage within the bag....

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Critical Recall: Glass Particulate in Pfizer Drugs

We recently reported on an FDA recall involving one lot of Bleomycin due to glass particulate matter found in the intravenous medication. The drug’s manufacturer,...

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Recall of IV Cancer Medication Due to Glass Particles

The FDA has announced an immediate recall of one lot of Bleomycin, an IV medication used to treat patients with cancer. The drug’s manufacturer, Hospira,...

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FDA Warning: Counterfeit Ozempic on the Market

In cooperation with Ozempic’s manufacturer, Novo Nordisk, the FDA has issued a stark warning about the presence of counterfeit Ozempic (semaglutide) injections on the market....

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