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Vehicle Safety

Vehicle Recalls320,000+ NHTSA safety recalls Browse VehiclesEvery make, model and year Complaints2.1M+ consumer safety complaints TSBs4.7M technical service bulletins VIN LookupDecode any vehicle VIN instantly OBD Codes12,000+ diagnostic trouble codes Fuel EconomyEPA MPG data for all vehicles Safety Ratings11,700+ NHTSA crash test ratings Investigations5,300+ NHTSA defect investigations StatisticsRecall trends & safety analysis Compare VehiclesTwo vehicles side by side

Consumer Safety

Product Safety9,700+ CPSC product recalls Food Safety28,600+ FDA food recalls Pet Safety1.3M FDA animal adverse events Drug Safety17,500+ FDA drug recalls Device Safety38,400+ FDA device recalls Workplace Safety102,900+ OSHA injury reports Brand HistoryRecall lookup by company

Infrastructure

Bridge Safety624,000 bridge inspections Aviation Safety30,000+ NTSB aviation events Dam Safety92,600 dam safety records Water Safety433,000+ public water systems Railroad Safety438,000+ rail crossings Pipeline Safety8,800+ pipeline incidents State DashboardsSafety grades for all 50 states ZIP ReportAny 5-digit ZIP across 9 datasets

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Browse Drug Recalls

1,110 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 1,110 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 1,110 FDA drug recalls in CA.

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DateProductReasonClassFirm
May 7, 2012 Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic ... Subpotent Drug: Salicylic acid is subpotent. Class III Guthy-Renker LLC
May 7, 2012 Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic ... Subpotent Drug: Salicylic acid is subpotent. Class III Guthy-Renker LLC
May 7, 2012 Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic ... Subpotent Drug: Salicylic acid is subpotent. Class III Guthy-Renker LLC
Apr 17, 2012 Loxitane Capsules, Loxapine Succinate Capsules, 10mg base, 100 count bottle,... Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used... Class III Watson Laboratories Inc
Apr 17, 2012 Loxapine Capsules USP, 25mg, 100 count bottle, Rx only, Manufactured By: Wats... Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used... Class III Watson Laboratories Inc
Apr 17, 2012 Loxapine Capsules USP, 10mg, 100 count bottle, Rx only, Manufactured By: Wats... Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used... Class III Watson Laboratories Inc
Apr 17, 2012 Loxapine Capsules USP, 50mg, 100 count bottle, Rx only Manufactured By: Watso... Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used... Class III Watson Laboratories Inc
Apr 17, 2012 Loxapine Capsules USP, 5mg, 100 count bottle, Rx only Manufactured By: Watson... Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used... Class III Watson Laboratories Inc
Dec 19, 2011 Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, ... Marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA... Class I Body Basics Inc
Mar 1, 2010 Eye Drops advanced relief (Dextran 70 0.1%, Polyethylene glycol 400 1%, Povid... Labeling: Label Mix-Up: Incorrect back labeling of the immediate container of eye drops (unit car... Class II K C Pharmaceuticals 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.