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Browse Drug Recalls

8 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 8 FDA drug recall enforcement actions. Each entry includes the product description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Drug Safety Recalls

Browse 8 FDA drug recalls.

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DateProductReasonClassFirm
Aug 31, 2018 Sore Throat & Laryngitis Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) pe... CGMP Deviations: products manufactured by contract manufacturer under conditions that could resul... Class II Beaumont Bio-med, Inc.
Aug 31, 2018 Muscle & Joint Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber... CGMP Deviations: products manufactured by contract manufacturer under conditions that could resul... Class II Beaumont Bio-med, Inc.
Aug 31, 2018 Arthritis Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glas... CGMP Deviations: products manufactured by contract manufacturer under conditions that could resul... Class II Beaumont Bio-med, Inc.
Aug 31, 2018 Colds & Flu Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass... CGMP Deviations: products manufactured by contract manufacturer under conditions that could resul... Class II Beaumont Bio-med, Inc.
Aug 31, 2018 Sinus Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral ... CGMP Deviations: products manufactured by contract manufacturer under conditions that could resul... Class II Beaumont Bio-med, Inc.
Aug 31, 2018 Allergy & Hay Fever Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber... CGMP Deviations: products manufactured by contract manufacturer under conditions that could resul... Class II Beaumont Bio-med, Inc.
Aug 31, 2018 Diarrhea Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass or... CGMP Deviations: products manufactured by contract manufacturer under conditions that could resul... Class II Beaumont Bio-med, Inc.
Aug 31, 2018 Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per ... CGMP Deviations: products manufactured by contract manufacturer under conditions that could resul... Class II Beaumont Bio-med, Inc.

Frequently Asked Questions

When a drug safety issue is identified — through FDA inspections, laboratory testing, adverse event reports, or manufacturer quality checks — the responsible company issues a recall to remove the affected products from the market. Pharmacies pull the product from shelves, and consumers are advised to contact their healthcare provider for alternatives.

The leading causes include cGMP deviations, impurity contamination (including nitrosamines like NDMA), failed dissolution or stability testing, sterility issues, potency problems, labeling errors, and foreign particle contamination.

Use the search and filter tools on this page to look up specific medications, active ingredients, or manufacturers. Each recall entry includes the product description, lot numbers, and distribution details.