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Browse Drug Recalls

7 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 7 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 7 FDA drug recalls.

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DateProductReasonClassFirm
Dec 3, 2021 CTx26 Kit, contains three tubes of CariFree CTx4 Gel 5000, 1.1% Neutral Sodiu... Subpotent Drug: Product contains less Sodium Fluoride than listed on product label. Class III Dental Alliance Holdings LLC
Dec 3, 2021 CTx36 Kit, contains three tubes of CariFree CTx4 Gel 5000, 1.1% Neutral Sodiu... Subpotent Drug: Product contains less Sodium Fluoride than listed on product label. Class III Dental Alliance Holdings LLC
Dec 3, 2021 CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g) Rx only... Subpotent Drug: Product contains less Sodium Fluoride than listed on product label. Class III Dental Alliance Holdings LLC
Dec 3, 2021 CTx21 Kit, contains three tubes of CariFree CTx4 Gel 5000, 1.1% Neutral Sodi... Subpotent Drug: Product contains less Sodium Fluoride than listed on product label. Class III Dental Alliance Holdings LLC
Dec 3, 2021 CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 GEl 5000 gel tubes. 1.... Subpotent Drug: Product contains less Sodium Fluoride than listed on product label. Class III Dental Alliance Holdings LLC
Dec 3, 2021 CariFree sample boxes, contains one tube of CariFree CTx4 Gel 5000, 1.1% Neut... Subpotent Drug: Product contains less Sodium Fluoride than listed on product label. Class III Dental Alliance Holdings LLC
Dec 3, 2021 CTx7 Kit, contains one tube CariFree CTx4 Gel 5000, 1.1% Neutral Sodium Fluor... Subpotent Drug: Product contains less Sodium Fluoride than listed on product label. Class III Dental Alliance Holdings LLC

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.