Medicines, 2014
Shortlist up to four to read them side by side.
1,562 medicine recalls FDA’s Enforcement Report published in 2014, 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.
1,562of 1,562 medicine recallsshown with your filters
The list
- Medicine recall Pleo Not PORTABLE SIPS 7X,10 x 1 mL Cartons, Oral Homeopathic Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Nota- Quent DROPS 5X, 10 mL Bottles, Homeopathic Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Quent SUPPOSITORIES 3X, 10 Suppository Cartons, Oral Homeopathic Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Quent CAPSULES 4X, 20 Capsule Cartons, Oral Homeopathic Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Quent DROPS 5X, 10 mL Bottles, Oral Homeopathic Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Quent PORTABLE SIPS 5X, 10 x 1 ml Cartons, Oral Homeopathic Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Fort SUPPOSITORIES 3X, 10 Suppository Carton, Homeopathic Digestive Aid Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Fort CAPSULES 4X, 20 Capsule Cartons Homeopathic Digestive Aid Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Fort PORTABLE SIPS 5X, 10 x 1 mL Carton Penicillin Cross Contamination. Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo-Fort DROPS 5X, 10ml bottle, Homeopathic Digestive Aid Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Fort TABLETS 5X, 20 Tablet Carton, Homeopathic Digestive Aid Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Ex SUPPOSITORIES 3X, 10 Suppository Packages Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Ex DROPS 5X, 10 ml bottles, Homeopathic Antifungal Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Ex PORTABLE SIPS 5X, 10 x 1 mL, Oral Homeopathic Medicine, OTC Only Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pleo Stolo DROPS 6X, 10ml Bottle Penicillin Cross Contamination Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Calcium Gluconate 10% for Injection, SDV 100 mL SDV, PF, Not for Dispensing, For Hospital Administration… Non-Sterility: RX Formulation initiated this recall due to a report of microbial contamination found in Calcium Gluconate saturated solution that was observed… FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 16, 2014in FDA’s Enforcement ReportArizonathe one state its words name PublishedApr 16, 2014ClassClass IStatusTerminatedWhereArizona
- Medicine recall Magnesium Sulfate 10gm Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices… Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportArizonathe one state its words name PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereArizona
- Medicine recall Potassium Phosphates 4.4mEq/3mM/mL Vials, Not for Dispensing, For Hospital Administration Only, Rx… Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices… Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportArizonathe one state its words name PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereArizona
- Medicine recall Oxytocin 30 Units Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices… Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportArizonathe one state its words name PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereArizona
- Medicine recall Sodium Bicarbonate 8.4%, a) 10 mL, b) 20 mL, and c) 22 mL units, Not for Dispensing, For Hospital… Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices… Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportArizonathe one state its words name PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereArizona
- Medicine recall Bupivacaine 3%, 300 mL units, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949… Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices… Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportArizonathe one state its words name PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereArizona
- Medicine recall Vitamin B-12 injections, a) 1 mL and b) 30 mL units, Not for Dispensing, For Hospital Administration Only, Rx… Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices… Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportArizonathe one state its words name PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereArizona
- Medicine recall Dr. Ming’s Chinese Capsule (Ginger 50 mg, Camellia Sinensis 50 mg, Malus Domestica 50 mg, Propetary Blend 300… Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and phenolphthalein. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Magic Slim capsules (Ling Zhi, Ebony, Fox-nut, Tuckahoe, Seman Pruni, Dioscoreae, Wheat Germ, Nature… Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and phenolphthalein. FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Dream Body Slimming Capsule (Chinese bitter orange 24%, Cassia Seed 18%, Aloe 16%, Lotus Leaf Extract 12%,… Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and . FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Vicerex A Powerful And Fast Acting Male Sexual Enhancer, 10 capsules per box, Dietary Supplement Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black… FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 16, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedApr 16, 2014ClassClass IStatusTerminatedWhereNo state named
- Medicine recall Black Ant, 4600 mg x 4 Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black… FDA Class I, its most serious class Class IFDA’s class (needs attention)Apr 16, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedApr 16, 2014ClassClass IStatusTerminatedWhereNo state named
- Medicine recall etomidate injection, USP, 2 mg/mL Presence of Particulate Matter: Potential for small black particles to be present in individual vials, the potential for missing lot number and/or expiry date… Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Demerol, meperidine HCL Inj Labeling; Missing label; ampoules are missing the immediate container label Class IIIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Ritalin HCl (methylphenidate HCl) USP, 10 mg, 100 tablets per Bottle Labeling: Incorrect or Missing Package Insert; The back of the Medication Guide attached to the Package Insert for Ritalin Tablets was printed with information… Class IIIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 16, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Ritalin HCl (methylphenidate HCl) USP, 20 mg, 100 tablets per Bottle Labeling: Incorrect or Missing Package Insert; The back of the Medication Guide attached to the Package Insert for Ritalin Tablets was printed with information… Class IIIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 16, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Ranitidine Tablets USP, 150 mg, 500-count bottles Presence of Foreign Tablets/Capsules: Recall is due to a pharmacist complaint of a “foreign material”, identified as Metoprolol Tartrate Tablet USP 50 mg,… Class IIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 16, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Spiriva HandiHaler (tiotropium bromide inhalation powder), Do Not Swallow Spiriva Capsules, For Use With… Defective Delivery System: Potential for dose delivery out of specification due to interation of the drug product powder with the lubricant on the interior of… Class IIIFDA’s classApr 16, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 16, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Duloxetine Delayed-Release Capsules, USP, 20 mg Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due… Class IIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedApr 9, 2014ClassClass IIStatusTerminatedWhereNationwide, and American Samoa, Guam, Puerto Rico and US Virgin Islands named
- Medicine recall Duloxetine Delayed-Release Capsules, USP, 30 mg Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due… Class IIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedApr 9, 2014ClassClass IIStatusTerminatedWhereNationwide, and American Samoa, Guam, Puerto Rico and US Virgin Islands named
- Medicine recall Duloxetine Delayed-Release Capsules, USP, 60 mg Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due… Class IIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedApr 9, 2014ClassClass IIStatusTerminatedWhereNationwide, and American Samoa, Guam, Puerto Rico and US Virgin Islands named
- Medicine recall Tivicay (dolutegravir) Tablets 50 mg, 30 Tablet Bottles Cross Contamination with Other Products: Product contains Promacta (eltrombopag). Class IIIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 9, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Suprax, Cefixime for Oral Suspension USP 500 mg/5 ml, 10mL (when reconstituted) Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station. Class IIIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 9, 2014ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Suprax, Cefixime for Oral Suspension USP, 500 mg/5 ml, 20 mL (when reconstituted) Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station. Class IIIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 9, 2014ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall HydrOXYzine HCl Tablets, USP 25 mg, 100 Tablet Blister Good Manufacturing Practices Deviations: The product has an active pharmaceutical ingredient from an unapproved source. Class IIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 9, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall HydrOXYzine HCl Tablets, USP 50 mg, 100 Tablet Blister Good Manufacturing Practices Deviations: The product has an active pharmaceutical ingredient from an unapproved source. Class IIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 9, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall QVAR¿ (beclomethasone dipropionate HFA), C4 INHALATION AEROSOL in Aluminum Cylinders, Mktd by: Teva… Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month stability time point Class IIIFDA’s classApr 9, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedApr 9, 2014ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops, 20 mL bottle Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm’s routine testing. Class IIIFDA’s classApr 2, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 2, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil), 4 fl Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm’s routine testing. Class IIIFDA’s classApr 2, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 2, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Body Oil) 4 fl Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm’s routine testing. Class IIIFDA’s classApr 2, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 2, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Body Oil) 4 fl Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm’s routine testing. Class IIIFDA’s classApr 2, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 2, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% (Scalp Oil), 4 fl.oz. Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm’s routine testing. Class IIIFDA’s classApr 2, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 2, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall ROYAL PHARMACEUTICALS DermOtic Oil fluocinolone acetonide 0.01% (Ear Drops), 20 ml Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm’s routine testing. Class IIIFDA’s classApr 2, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedApr 2, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
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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