Medicines, 2019
Shortlist up to four to read them side by side.
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 5, 2026.
2,152of 2,152 medicine recallsshown with your filters
The list
- Medicine recall S-TESTOSTERONE CYP 200MG/ML MDV In SESAME OIL Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TEST CYP/NAN-DECA 200/50MG/ML MDV IN SESAME OIL Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TEST CYP/PROP 160/40MG/ML MDV IN ETHYL OLEATE Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TEST CYP/PROP/DECA-NAN 250MG/ML Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TEST CYP/PROP 160/40MG/ML MDV IN SESAME OIL Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TESTOSTERONE PROPIONATE 100MG/ML MDV IN SESAME OIL Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TESTOSTERONE ULTRA 250MG/ML MDV IN SESAME OIL (TEST CYP 200MG/TEST PROP 25MG/NANDROLONE DECA 25MG) Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-VIT B COMPLEX INJ SOLN (HP) Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TRIMIX (15MG/0.5MG/16MCG/ML) INJ, Rx Only, 5ML glass vial. Red Mountain Compounding Rx. Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TRIMIX (40MG/2.5MG/29MCG) MDV INJ; Rx Only, 5ml glass vial, Red Mountain Compounding Rx Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TRIMIX (29.4MG/0.98MG/9.8MCG/ML) INJ; Rx Only, 5ml glass vial. Red Mountain Compounding Rx Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall S-TRIMIX various strengths to include:a) S-TRIMIX Lack of Assurance of Sterility Class IIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Sankaijo BOTANICAL LAXATIVE (docusate sodium 8.33 mg and sennosides 1.36 mg) tablets, 150-count bottles Subpotent Drug: Formulated amount of sennosides component is less than labelled claim. Class IIIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedNov 13, 2019ClassClass IIIStatusTerminatedWhereNationwide, and Guam and Northern Mariana Islands named
- Medicine recall Cephalexin for Oral Suspension USP, 250 mg/5mL, 200 mL bottle Presence of Foreign substance: identified as a dead ant. Class IIIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Cefdinir for Oral Suspension USP, 250 mg/5mL,100 mL bottle Presence of Foreign substance: identified as a dead ant. Class IIIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Cefdinir for Oral Suspension USP, 125 mg/5mL Presence of Foreign substance: identified as a dead ant. Class IIIFDA’s classNov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall LACTATED RINGER’S Injection, USP, 500 mL flexible container Presence of Particulate Matter. FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IStatusTerminatedWhereNationwide
- Medicine recall 0.9% SODIUM CHLORIDE INJECTION, USP, 250 mL VisIV Container Presence of Particulate Matter. FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 13, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 13, 2019ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Green Lumber Natural Fuel For Men capsule Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain undeclared Tadalafil, an FDA approved drug for the treatment of erectile… FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 13, 2019in FDA’s Enforcement ReportNot namedno state, in where it went PublishedNov 13, 2019ClassClass IStatusTerminatedWhereNo state named
- Medicine recall Atorvastatin Calcium Tablets, USP 40 mg*, 1,000 count bottles Presence of Foreign Tablets/Capsules: a single tablet of Pravastatin 40 mg found in bottle of Atorvastatin Calcium 40 mg. Class IIIFDA’s classNov 6, 2019in FDA’s Enforcement Report5 statesnamed in where it went PublishedNov 6, 2019ClassClass IIIStatusTerminatedWhereIllinois, Mississippi, New Jersey, Ohio and Texas
- Medicine recall PF-Succinylcholine Chloride Injection, USP 20 mg/mL Incorrect labeling: Incorrect or missing lot and/or exp date Class IIIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Prasugrel Tablets 5 mg, 30-count bottles Failed Dissolution Specification: Low out of specification dissolution results. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Estradiol Vaginal Inserts USP, 10 mcg Defective Delivery System: complaints for difficulty in pushing the plunger of the applicator. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lyophilized Chorionic Gonadotropin 11,000 USP Units for Injection Lack of Sterility Assurance. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lyophilized Human Chorionic Gonadotropin 5,000 USP Units For injection Lack of Sterility Assurance. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lyophilized Sermorelin w/ GHRP2 3 mg For injection Lack of Sterility Assurance. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Lyophilized Human Chorionic Gonadotropin 5,500 USP Units For injection Lack of Sterility Assurance. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Bimatoprost Ophthalmic Solution 0.03% Labeling: Incorrect or missing package insert. Class IIIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension Labeling: Incorrect or missing package insert. Class IIIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Gatifloxacin Ophthalmic Solution 0.5%, For Use in the Eyes Only Labeling: Incorrect or missing package insert. Class IIIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall AVKARE Ranitidine Hydrochloride Capsules 150 mg 500 Capsules CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API Class IIFDA’s classNov 6, 2019in FDA’s Enforcement Report2 statesnamed in where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereColorado and Missouri
- Medicine recall AVKARE Ranitidine Hydrochloride Capsules 300 mg 500 Capsules CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API Class IIFDA’s classNov 6, 2019in FDA’s Enforcement Report2 statesnamed in where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereColorado and Missouri
- Medicine recall Ranitidine Tablets USP,150 mg, 8-count bottles CGMP DEVIATIONS: One lot of Ranitidine Tablets USP, 150 mg is being recalled because some bottles were empty. Class IIIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIIStatusOngoingWhereNationwide
- Medicine recall Testosterone Cypionate Injection, USP, 2000 mg/10 mL, 1 mL Vial, Single-Dose Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate Injection, USP, 200mg/mL, 1 ml single-dose vials, found to contain shelf cartons labelled… Class IIIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Ibuprofen Oral Suspension USP, 100 mg/5 mL, 4 fl Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Ibuprofen Oral Suspension USP, 100 mg/5 mL, One Pint Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Children’s Ibuprofen Oral Suspension USP, 100 mg per 5 mL, Berry Flavor, Dye-Free, Alcohol Free, 4 fl Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Children’s Ibuprofen Oral Suspension USP, 100 mg per 5 mL, Berry Flavor, Dye-Free, Alcohol Free, 8 fl Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Children’s Ibuprofen Oral Suspension USP, 100 mg per 5 mL, Berry Flavor, Dye-Free, Alcohol Free, 4 fl Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing. Class IIFDA’s classNov 6, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 6, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Mero Macho Artificially Flavored Passion Fruit Vitamin C Liquid Supplement, 2.04 fl oz Marketed without an approved NDA/ANDA: Product found to be tainted with Tadalafil. FDA Class I, its most serious class Class IFDA’s class (needs attention)Nov 6, 2019in FDA’s Enforcement Report3 statesnamed in where it went PublishedNov 6, 2019ClassClass IStatusTerminatedWhereFlorida, New York and Pennsylvania
- Medicine recall PF-Fentanyl Citrate GMP Deviations: potential glass contamination Class IIFDA’s classOct 30, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 30, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% GMP Deviations: potential glass contamination Class IIFDA’s classOct 30, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 30, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% GMP Deviations: potential glass contamination Class IIFDA’s classOct 30, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 30, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Amino Acid Injection 50 g/1000 mL Lack of Assurance of Sterility; bags have potential to leak Class IIFDA’s classOct 30, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 30, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container Lack of Assurance of Sterility; bags have potential to leak Class IIFDA’s classOct 30, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 30, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416… Lack of sterility assurance. Class IIFDA’s classOct 30, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 30, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Pioglitazone Hydrochloride Tablets USP 15 mg, 30 count bottles Superpotent Class IIFDA’s classOct 23, 2019in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 23, 2019ClassClass IIStatusTerminatedWhereNo state named
- Medicine recall Fentanyl Citrate USP, Active Pharmaceutical Ingredient, Spectrum Chemical MFG CGMP Deviations: Received notice from supplier that there is potential glass contamination. Class IIFDA’s classOct 23, 2019in FDA’s Enforcement Report4 statesnamed in where it went PublishedOct 23, 2019ClassClass IIStatusTerminatedWhereCalifornia, Colorado, Maryland and South Carolina
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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