Medicines, 2024
Shortlist up to four to read them side by side.
657 medicine recalls FDA’s Enforcement Report published in 2024, newest first; 18,075 in all since 2012.
FDA’s medicine recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 5, 2026.
657of 657 medicine recallsshown with your filters
The list
- Medicine recall TraMADol HCl 50 mg Tablet Presence of Foreign Tablets: Manufacturer received a report from a Pharmacist who reported finding a tablet of baclofen in a bottle of 1000-count tramadol Class IIFDA’s classMay 15, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 15, 2024ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Sodium Sulfacetamide 10% - Sulfur 5% Cleanser Subpotent drug Class IIIFDA’s classMay 15, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 15, 2024ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Clorazepate Dipotassium Tablets, USP, 3.75 mg, a) 100 tablets per bottle Discoloration: Dotted and yellow spots on tablets Class IIFDA’s classMay 15, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 15, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall Clorazepate Dipotassium Tablets, USP, 7.5 mg, a) 100 tablets per bottle Discoloration: Dotted and yellow spots on tablets Class IIFDA’s classMay 15, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 15, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall Amphotericin B Liposome for Injection, 50mg vials Out of specification for assay Class IIFDA’s classMay 15, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 15, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic Solution 1%, 0.5%, 0.075%, 8mL,… Subpotent Drug Class IIFDA’s classMay 8, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 8, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall Methylergonovine Maleate Tablets, USP, 0.2mg, 12-count bottle Failed Dissolution Specifications Class IIFDA’s classMay 8, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 8, 2024ClassClass IIStatusCompletedWhereNationwide
- Medicine recall Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free, 1 mL Single-Use vials Out of specification for assay Class IIIFDA’s classMay 8, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 8, 2024ClassClass IIIStatusOngoingWhereNationwide
- Medicine recall EYLEA, (aflibercept) Injection, 2 mg Lack of Assurance of Sterility: Complaints of syringe breakage Class IIFDA’s classMay 8, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 8, 2024ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Fentanyl 1000mcg/100mL Labeling: Wrong Barcode Class IIIFDA’s classMay 8, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 8, 2024ClassClass IIIStatusCompletedWhereNationwide
- Medicine recall Valacyclovir Tablets USP, 500 mg, 90 count bottles Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets. Class IIIFDA’s classMay 8, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 8, 2024ClassClass IIIStatusCompletedWhereNationwide
- Medicine recall Spanish Fly 22K capsules, 2-count box Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall Weiner Boner Honey, 12g packet, 100% Organic Formula. Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall Flower Power, CBD infused Female Enhancement, 59 ml bottle Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall Samurai-X Honey 6800 Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall Pink Pussycat Honey Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall libigrow RED DRAGON+, Maximum Strength Formula, 2 capsules per box Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall SILVERBACK XXX POWER MALE ENHANCEMENT, 2 fl Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall The GOAT SUBLINGUAL STRIP, MALE ENHANCEMENT, 2 Pack Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall ALPHASTRIP MALE PERFORMANCE ENHANCER, The fastest acting sublingual, Serving Size Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall HONEY MANUKA BUNNY LOVE, 12g, All Natural Sexual Enhancement Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall Alcoholada Gel, Pain Relieving Gel, 0.5% Lidocaine Hydrochloride Chemical Contamination: Product manufactured with ethanol API that contains methanol FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall Aruba Aloe Hand Sanitizer Gel, 80% Alcohol, 12 fl oz Chemical Contamination: Product manufactured with ethanol API that contains methanol FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusOngoingWhereNationwide
- Medicine recall Eyesaline, Saline Eyewash Solution, Cartridge for Fendall 2000, Net contents: 7.9 gal per cartridge, Sperian… CGMP Deviations Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall GloStrips, Fluorescein Sodium Ophthalmic Strips USP Failed Impurities/Degradation Specifications: The Active Pharmaceutical Ingredient (API) used in the product is not being manufactured to the current USP… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall GloStrips, Fluorescein Sodium Ophthalmic Strips USP Failed Impurities/Degradation Specifications: The Active Pharmaceutical Ingredient (API) used in the product is not being manufactured to the current USP… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall FUL-GLO, Fluorescein Sodium Sterile Ophthalmic Strips USP Failed Impurities/Degradation Specifications: The Active Pharmaceutical Ingredient (API) used in the product is not being manufactured to the current USP… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall FUL-GLO, Fluorescein Sodium Ophthalmic Strips USP 1 mg, 100 sterile strips per carton Failed Impurities/Degradation Specifications: The Active Pharmaceutical Ingredient (API) used in the product is not being manufactured to the current USP… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall Abilify (aripiprazole), 5 mg tablets Cross Contamination with Other Products Class IIIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIIStatusOngoingWhereNationwide
- Medicine recall Abilify (aripiprazole), 10 mg tablets Cross Contamination with Other Products Class IIIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIIStatusOngoingWhereNationwide
- Medicine recall Abilify (aripiprazole), 15 mg tablets Cross Contamination with Other Products Class IIIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIIStatusOngoingWhereNationwide
- Medicine recall Abilify (aripiprazole), 30 mg tablets Cross Contamination with Other Products Class IIIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIIStatusOngoingWhereNationwide
- Medicine recall ForeverMen Natural Energy Boost Capsules Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of… FDA Class I, its most serious class Class IFDA’s class (needs attention)May 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Ipratropium Bromide and Albuterol Sulfate Inhalation Solution USP, 0.5 mg & 3mg/3mL unit-dose vials Short fill: Complaints received of less fill volume in respule and few drops of liquid observed in the intact pouch. Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle Failed Dissolution Specifications Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusOngoingWhereNationwide
- Medicine recall Cloderm (clocortolone pivalate) Cream, 0.1% CGMP Deviation: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall minolira (minocycline hydrochloride) extended-release tablets, 105mg 30-count Bottle CGMP Deviation: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall minolira (minocycline hydrochloride) extended-release tablets, 135mg 30-count Bottle CGMP Deviation: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity… Class IIFDA’s classMay 1, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 1, 2024ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall NEXLIZET (bempedoic acid and ezetimibe) tablets, 180 mg/10 mg, 30-count bottle Failed dissolution specifications: out-of-specification bempedoic acid dissolution at the 0-month timepoint. Class IIIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIIStatusCompletedWhereNationwide
- Medicine recall Vancomycin Hydrochloride for Oral Solution, USP, 250 mg per 5 mL Superpotent Drug: Due to overfilling of drug powder FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Digoxin Tablets, USP 62.5 mcg Failed Impurities/Degradation Specifications Class IIIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Atovaquone Oral Suspension USP, 750 mg per 5 mL sachets, 20 Units x 5 mL cartons Microbial contamination of a non-sterile product: potential Bacillus cereus contamination. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Sterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGULAR (insulin human injection),… CGMP Deviations Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusCompletedWhereNationwide
- Medicine recall S.P.Labs, Thyroid, Full Strength Failed Stability Specifications Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusCompletedWhereNationwide
- Medicine recall S.P Labs, Thyroid, USP Failed Stability Specifications Class IIFDA’s classApr 24, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 24, 2024ClassClass IIStatusCompletedWhereNationwide
- Medicine recall Rifampin Capsules USP, 300mg, 30-count bottles Subpotent Drug Class IIFDA’s classApr 17, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 17, 2024ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14… CGMP Deviations Class IIFDA’s classApr 17, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 17, 2024ClassClass IIStatusTerminatedWhereNationwide
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Drug recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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