Medicines, 2018
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1,426 medicine recalls FDA’s Enforcement Report published in 2018, 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.
1,426of 1,426 medicine recallsshown with your filters
The list
- Medicine recall HYDROXOCOBALAMIN Injectable-30 mL MDV Presence of Particulate matter. Class IIFDA’s classMay 2, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 2, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall LIPO-B Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532 Presence of Particulate matter. Class IIFDA’s classMay 2, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 2, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall LIPO-DEN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532 Presence of Particulate matter. Class IIFDA’s classMay 2, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 2, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall LIPO-DEN EXTREME Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532 Presence of Particulate matter. Class IIFDA’s classMay 2, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 2, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall LIPO-DEN PLUS Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532 Presence of Particulate matter. Class IIFDA’s classMay 2, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 2, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall LIPO-PLEX Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532 Presence of Particulate matter. Class IIFDA’s classMay 2, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 2, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall METHYLCOBALAMIN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532 Presence of Particulate matter. Class IIFDA’s classMay 2, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 2, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall PYRIDOXINE Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532 Presence of Particulate matter. Class IIFDA’s classMay 2, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 2, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours Defective Delivery System: Out of specification for adhesive transfer. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall PASTA DE LASSAR ANDROMACO Skin Protection, 25% zinc oxide Topical cream, 60 gram tube Microbial Contamination of Non-Sterile Products Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportTexasthe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereTexas
- Medicine recall ACURE, clarifying acne, glycolic + zinc (salicyclic acid 0.5%) towelettes, 30-count pouch CGMP Deviations: finished products were manufactured with poor quality water. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches, Dist CGMP Deviations: finished products were manufactured with poor quality water. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles Cross Contamination With Other Products: presence of unrelated ingredients (i.e. Class IIIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 25, 2018ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP cGMP deviations Class IIIFDA’s classApr 25, 2018in FDA’s Enforcement Report2 statesnamed in where it went PublishedApr 25, 2018ClassClass IIIStatusTerminatedWhereMassachusetts and Washington
- Medicine recall Amantadine HCl Capsules, USP, 100 mg, 50 Capsules Failed Dissolution Specifications Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Ascorbic Acid (Tapioca) 500 mg/mL, 50 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall B-complex (B1-200mg, B2-4mg, B3-200mg,B5-4mg,B6-4mg) /mL, 5 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Biotin Suspension 10mg/mL, 5 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall CoEnzymeQ10 25mg/mL, 5mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Glutathione 200mg/mL, 10mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall HCG 1000 units/mL Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Lipoic Acid 25mg/mL, 5 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Methionine15mg/Inositol 50mg/Choline 100mg Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Nandrolone decanoate 200mg/mL, 5 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone Cypionate 200mg/mL, 5 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall TM #1 (ALP 5.9/PAPAV 17.65/PHEN 0.59) Injectable solution Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Vitamin D 50,000 unit/ml, 5 mL amber vial, Injectable Liquid Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg, 50 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Naltrexone 200 mg pellet, amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Pregnenolone 100 mg (SD) pellet, amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Progesterone 50 mg (SD) pellets in amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone/Anastrozole 120 mg/8 mg pellets Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone/Estradiol 60 mg/6 mg pellet Amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone/Finasteride 60 mg/5 mg pellet Amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg pellet Amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Methylcobalamin 12.5 mg/mL, Injectable Liquid Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall MVI-7 (B1-100mg/B3-100mg, B5-252 mg, B6-102mg, Vit C-2500 mg, B12-10mg, Mag-1000 mg)/ vial liquid injectable,… Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone Propionate 100mg/mL, 5 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall TM #4 (ALP 20/PAPAV/PHENT 2), 3 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall TM #6 (ALP 25/PAPAV/PHENT1), 3 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall TM (ALP 50/PAPAV 30/PHENT1.5 mg), 3 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall TM #3 (ALP10/PAPAV12/PHENT1), 3 mL amber vial Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone 200 mg pellet Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone 100 mg pellet Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone 25 mg pellet Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone 37.5 mg pellet Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
- Medicine recall Testosterone 40 mg pellet Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. Class IIFDA’s classApr 25, 2018in FDA’s Enforcement ReportNevadathe one state its words name PublishedApr 25, 2018ClassClass IIStatusTerminatedWhereNevada
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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