Medicines, 2019
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2,152 medicine recalls FDA’s Enforcement Report published in 2019, 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 6, 2026.
2,152of 2,152 medicine recallsshown with your filters
The list
- Medicine recall RAMUCIRUMAB 457 MG QS 250 ML NS IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall REMICADE 680 MG QS 250 ML 0.9% NACL IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall RITUXAN 728 MG QS 728 mL 0.9% NACL IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall RITUXIMAB 575 MG / 250 ml 0.9% NACL IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall RomiPLOStim 700 MCG/ 1.4 ML SQ SYR Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall Sodium Chloride 0.9% 1 LITER WITH Potassium Chloride 20 mEq, Mannitol 12.5 G, Magnesium Sulfate 2 G Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall SOLIRIS 1200 MG QS 240 ML NACL0.9% IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall TOPOTECAN 1.24 MG / 100 ML NS IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall TRASTUZUMAB 427 MG / 250 ml NS IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall VELCADE 2.1 mg / 0.84 ml SQ SYRINGE Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall VINBLASTINE 10.9 MG / 100 ML D5W IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall VINCRISTINE 1 MG /50 ML NS IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall FERRIC CARBOXYMALTOSE 750mg/50ml NS IVPB Lack of Assurance of Sterility Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNew York
- Medicine recall Aspirin and Extended-release Dipyridamole Capsules, 25 mg/200 mg, 20 capsules per carton Failed Impurities/Degradation Specifications; out of specification result for an unknown impurity in stability samples. Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Carbamazepine, Extended-Release Tablets, USP, 400 mg, 30 Tablets Failed Dissolution Specifications Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Tamsulosin Hydrochloride Capsules, USP 0.4 mg Failed Dissolution Specifications Class IIFDA’s classAug 21, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 21, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lovastatin Tablets USP, 40 mg CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results. Class IIIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 14, 2019ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Smart Sense Regular Strength Aspirin Tablets, 325 mg Labeling; Incorrect or Missing Lot Number and/or Exp Date; Product has an incorrect expiration date of 9/2022 applied to the labeling, where the actual… Class IIIFDA’s classAug 14, 2019in FDA’s Enforcement ReportKansasthe one state its words name PublishedAug 14, 2019ClassClass IIIStatusTerminatedWhereKansas
- Medicine recall Mometasone Furoate Cream USP, 0.1% GMP Deviations: Glenmark received complaints stating that mometasone fuorate cream was gritty. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Asma Aid Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808 CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Asthma Balm 60 gram CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Awake, 500 mg Capsules, 90-count bottles CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Baby Saver Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Bone Fixer, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808 CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800)… CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Deafness Off Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Dragon Pain Balm CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Dragon Pain Oil CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Edema Off Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Fungo Balm, 30 gram, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808 CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Glauco-Catar Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Hair Back, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800)… CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Herpes-G Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Herpes-P, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800)… CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Herpes-S, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800)… CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Herpes-V Balm CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lipidtrol Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lube Lax Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lump Off Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lung Fixer Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lung Saver Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lung Tonic EX Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Migraine Off Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pain Away, 500 mg Capsules, 90-count bottles CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pain Stopper, 500 mg Capsules, 90-count bottles CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Prostatin Capsules CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Psoriasis Balm, 60 gram, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808 CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Sperm Booster CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Class IIFDA’s classAug 14, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 14, 2019ClassClass 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.
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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