December 4, 2024

Man of Steel Recalling Supplements for Undeclared Drug

Man of Steel is voluntarily recalling 175 lots of Man of Steel 1 and Man of Steel 2 because they contain undeclared Sildenafil. The FDA has issued a risk statement, “The product has/potentially could result in death. The groups affected are men with diabetes, high blood pressure, high cholesterol, or heart disease. Man of Steel has received reports from the FDA lab but not received any reports of adverse events related to this recall.”

The product is packaged in an individual blister package. The capsules are 4000 mg. The expiration dates of the recalled products are 10-17-18. It was distributed throughout local convenience stores in Sacramento, California.

Two other advisories about these products were issued by the FDA on June 22, 2017. Sildenafil is the active ingredient in Viagra.

If you purchased this product, stop using it immediately. Return it to the place of purchase, or discard it in accordance with your community’s drug disposal policies. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program.

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