Medicines, 2020
Shortlist up to four to read them side by side.
1,035 medicine recalls FDA’s Enforcement Report published in 2020, 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.
1,035of 1,035 medicine recallsshown with your filters
The list
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 9 mcg and levothyroxine (T4) 38 mcg], 1 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 6.75 mcg and levothyroxine (T4) 28.5 mcg], 3/4 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 4.5 mcg and levothyroxine (T4) 19 mcg], 1/2 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 11.25 mcg and levothyroxine (T4) 47.5 mcg], 1.25 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 13.5 mcg and levothyroxine (T4) 57 mcg], 1.5 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 15.75 mcg and levothyroxine (T4) 66.5 mcg], 1.75 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 18 mcg and levothyroxine (T4) 76 mcg], 2 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 20.25 mcg and levothyroxine (T4) 85.5 mcg], 2.25 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 22.5 mcg and levothyroxine (T4) 95 mcg], 2.5 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Nature-Throid, Thyroid USP [liothyronine (T3) 27 mcg and levothyroxine (T4) 114 mcg], 3 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, Thyroid USP, [liothyronine (T3) 2.25 mcg and levothyroxine (T4) 9.5 mcg], 1/4… CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, 1/2 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, 3/4 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, 1 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, 1.25 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, 1.5 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, 1.75 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, 2 Grain CGMP Deviations: manufactured under the same conditions as those found to be subpotent. Class IIFDA’s classSep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall WP Thyroid, Westhroid Pure, 1/2 Grain Subpotent Drug: FDA analysis found product to be subpotent FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Nature Throid, 1/2 Grain Subpotent Drug: FDA analysis found product to be subpotent FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Nature Throid, 3/4 Grain Subpotent Drug: FDA analysis found product to be subpotent FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Nature Throid, 1.25 Grain Subpotent Drug: FDA analysis found product to be subpotent FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Nature Throid, 2 Grain Subpotent Drug: FDA analysis found product to be subpotent FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Nature Throid, 1.5 Grain Subpotent Drug: FDA analysis found product to be subpotent FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 23, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 23, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Cephalexin for Oral Suspension, USP 125 mg per 5 mL, For Reconstitution, For Oral Use Only CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits. Class IIFDA’s classSep 16, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedSep 16, 2020ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Cephalexin for Oral Suspension, USP 250 mg per 5 mL, For Reconstitution, For Oral Use Only CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits. Class IIFDA’s classSep 16, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedSep 16, 2020ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Vancomycin HCL 1.5 mg Edge Pharma, LLC 856 Hercules Dr Labeling: Label Error on Declared Strength Class IIFDA’s classSep 16, 2020in FDA’s Enforcement ReportWisconsinthe one state its words name PublishedSep 16, 2020ClassClass IIStatusTerminatedWhereWisconsin
- Medicine recall Always Be Clean Hand Sanitizer Labeling Not Elsewhere Classified: Product labeled to contain methanol Class IIFDA’s classSep 16, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 16, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count Labeling Not Elsewhere Classified: Product labeled to contain methanol Class IIFDA’s classSep 16, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 16, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Shine & Clean Hand Sanitizer gel, (Ethyl Alcohol 70%), 33.81 fl oz CGMP Deviations: Products manufactured at the same site were FDA testing found below the label claim for ethanol content and the presence of undeclared… Class IIFDA’s classSep 16, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 16, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Cephalexin for Oral Suspension, USP 250 mg per 5 mL, For Reconstitution, For Oral Use Only Sub-Potent Drug: Out of specification test results for potency (below specification). Class IIFDA’s classSep 16, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedSep 16, 2020ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% with Vitamin E cGMP deviations Class IIFDA’s classSep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall UltraCruz Hand Sanitizing Gel Antimicrobial Subpotent drug Class IIFDA’s classSep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall HGH Vitality Homeopathic, 90 tablets Labeling: Error on Declared Strength Class IIFDA’s classSep 9, 2020in FDA’s Enforcement ReportUtahthe one state its words name PublishedSep 9, 2020ClassClass IIStatusTerminatedWhereUtah
- Medicine recall Command Brands GelAnti Bac Instant Hand Sanitizer, 70% Alcohol, , 8 FL OZ 250mL bottle, Roqueplast S.A CGMP Deviation: Potential contamination with undeclared methanol. Class IIFDA’s classSep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Bersih Hand Sanitizer Gel cGMP Deviations Class IIFDA’s classSep 9, 2020in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 9, 2020ClassClass IIStatusTerminatedWhereNo state named
- Medicine recall Leiper’s Fork Distillery, Alcohol Antiseptic Topical Solution, Ethyl Alcohol 70% Labeling Not Elsewhere Classified: Product labeled to contain methanol. Class IIFDA’s classSep 9, 2020in FDA’s Enforcement ReportTennesseethe one state its words name PublishedSep 9, 2020ClassClass IIStatusTerminatedWhereTennessee
- Medicine recall bio aaa Advance Hand Sanitizer Ethyl Alcohol 70%, Unscented, 16.23 Oz CGMP Deviations Class IIFDA’s classSep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall bio aaa Advance Hand Sanitizer Ethyl Alcohol 70%, Unscented, 16.23 Oz Chemical Contamination: Product contains methanol. FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall SkinGuard 24 All-Day Hand Sanitizer 2.67 oz Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall SkinGuard 24 All-Day Hand Sanitizer 8 oz Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC, Bolingbroke, GA 31004 Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Skin Guard 24 All-Day Hand Sanitizer 1 4”x6” Hand Sanitizing Towelette Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Amiodarone Hydrochloride Injection, USP, 450 mg/9 mL Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid Injection, USP to contain vials of Amiodarone HCl Injection, USP and cartons labeled… FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Tranexamic Acid Injection, USP, 1000 mg/10 mL Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid Injection, USP to contain vials of Amiodarone HCl Injection, USP and cartons labeled… FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 9, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 9, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Buprenorphine HCl Injection, 0.3 mg/mL, 1 mL vial, For Intramuscular or Intravenous Use Only Sub-potent Drug: Out-of-Specification assay results found at 3 month stability testing. Class IIFDA’s classSep 2, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 2, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Chlorhexidine Gluconate 0012 For Manufacturing, Processing or Repacking Microbial contamination of Non-Sterile Product; detection of the gram-negative bacillus Serratia marcescens in certain API batches FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 2, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 2, 2020ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Sulfamethoxazole and Trimethoprim Tablets, USP, 800 mg/160 mg Double Strength, 500 Tablets per bottle Presence of Foreign Substance: product complaints were received by the firm for the presence of metal wire in the tablet(s). Class IIFDA’s classSep 2, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 2, 2020ClassClass 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.”
Your shortlist0 of 4
Add one more to compare.