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Browse Drug Recalls

13 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 13 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 13 FDA drug recalls.

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DateProductReasonClassFirm
Jul 15, 2022 Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Cherry Flavor, 10 ... CGMP Deviations Class II Vi-Jon, LLC
Jul 15, 2022 SWAN, Citroma MAGNESIUM CITRATE, Saline Laxative, Oral Solution, (1.745 g/fl ... Microbial contamination of non-sterile products. Class I Vi-Jon, LLC
Jul 15, 2022 Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon Flavor, 10 F... CGMP Deviations Class II Vi-Jon, LLC
Jun 28, 2022 Hydrogen Peroxide Topical Solution USP, 3%, 16 FL OZ (1 PT) 473 mL bottle, pa... Cross Contamination With Other Products: Product is cross contaminated with low levels of isoprop... Class II Vi-Jon, LLC
Mar 2, 2022 HEB 50% Isopropyl Alcohol First Aid Antiseptic, packaged in 16 FL OZ 91 PT) 4... Labeling: Label Mix-Up-The primary label on the front of the bottles have 50% Isopropyl Alcohol a... Class II Vi-Jon, Inc.
Sep 9, 2021 Kroger 70% Isopropyl Alcohol First Aid Antiseptic 32 FL OZ (1 QT) 946 mL 5 Di... Labeling: Label Mix-Up.The recall has been initiated after receiving one complaint about incorrec... Class II Vi-Jon, Inc.
Feb 20, 2019 Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Ag... Cross Contamination: Presence of IPA in finished product. Class II Vi-Jon, Inc.
Sep 13, 2017 Magnesium Citrate Oral Solution Lemon Flavor, 1.745g per fl oz, packaged in ... Failed Impurities/Degradation Specifications. Class III Vi-Jon, Inc.
Sep 13, 2017 Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) Distribute... Failed Stability Specifications Class III Vi-Jon, Inc.
Sep 13, 2017 Magnesium Citrate Oral Solution Cherry Flavor, 1.745 g per fl oz, packaged in... Failed Impurities/Degradation Specifications. Class III Vi-Jon, Inc.
Jul 17, 2017 Magnesium Citrate Oral Solution, packaged in a 10 fl. oz. (296 mL) glass bott... Microbial contamination of non-sterile products: product was found to contain mold, identified as... Class II Vi-Jon, Inc.
Jun 12, 2017 Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. ... Presence of foreign substance: glass particle Class II Vi-Jon, Inc.
Jul 18, 2013 ALCOHOL FREE ANTISEPTIC (cetylpyridinium chloride) Mouth Rinse, 0.07%, mint, ... Microbial Contamination of Non-Sterile Products: This product is being recalled because a stabili... Class III Vi-Jon, 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.