Medicines, 2017
Shortlist up to four to read them side by side.
1,073 medicine recalls FDA’s Enforcement Report published in 2017, 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.
1,073of 1,073 medicine recallsshown with your filters
The list
- Medicine recall Trimix Injectable 30 mg/3 mg/100 mcg/mL, a) 5 mL and 10 mL vials, Compounded by Wells Pharmacy, Ocala, FL Lack of Assurance of Sterility Class IIFDA’s classJan 11, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 11, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Trimix Injectable 30 mg/3 mg/60 mcg/mL, a) 2 mL, b) 5 mL and c) 10 mL vials, Compounded by Wells Pharmacy,… Lack of Assurance of Sterility Class IIFDA’s classJan 11, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 11, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Tri-Test 200 (CEP 100-75-25) Injectable, 200 mg/mL, 10 mL vial, Compounded by Wells Pharmacy, Ocala, FL Lack of Assurance of Sterility Class IIFDA’s classJan 11, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 11, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Vitamin D3 in Sesame Oil Injectable 100,000 IU/mL, 5 mL, vial, Compounded by Wells Pharmacy, Ocala, FL Lack of Assurance of Sterility Class IIFDA’s classJan 11, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 11, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Vitamin D3 in Sesame Oil Injectable 50,000 IU/mL, 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL Lack of Assurance of Sterility Class IIFDA’s classJan 11, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 11, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Testosterone Cypionate in Grapeseed Oil Injectable, (NY STATE), 200 mg/mL, 10 mL vial, Compounded by Wells… Lack of Assurance of Sterility Class IIFDA’s classJan 11, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 11, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Testosterone Cypionate in Sesame Oil Injectable, (NY STATE), 200 mg/mL, 10 mL vial, Compounded by Wells… Lack of Assurance of Sterility Class IIFDA’s classJan 11, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 11, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall CVS Health Homeopathic Infants Teething Tablets 135 count bottle CGMP Deviations Class IIFDA’s classJan 4, 2017in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedJan 4, 2017ClassClass IIStatusTerminatedWhereNew York
- Medicine recall Kids’ Relief Ear Relief Oral Liquid 0.85 fl oz. CGMP Deviations Class IIFDA’s classJan 4, 2017in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedJan 4, 2017ClassClass IIStatusTerminatedWhereNew York
- Medicine recall CVS pharmacy Kids’ Ear Relief Oral Liquid 0.85 oz CGMP Deviations Class IIFDA’s classJan 4, 2017in FDA’s Enforcement ReportNew Yorkthe one state its words name PublishedJan 4, 2017ClassClass IIStatusTerminatedWhereNew York
- Medicine recall Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or has illegible lot and expiry codes, as well as defective or cracked caps. Class IIIFDA’s classJan 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 4, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Nadolol Tablets, USP, 40mg Failed dissolution specification: recalled due to an out of specification dissolution result of 40% (Specification: NLT 80%) Class IIFDA’s classJan 4, 2017in FDA’s Enforcement Report2 statesnamed in where it went PublishedJan 4, 2017ClassClass IIStatusTerminatedWhereMississippi and Ohio
- Medicine recall INOVA (benzoyl peroxide) 4%, Easy Pad (tocopherol) 5%, For topical use only Subpotent Drug: Product label claim is 4% Benzoyl Peroxide, Initial Stability testing showed variation within the lot outside of product specifications. Class IIIFDA’s classJan 4, 2017in FDA’s Enforcement Report3 statesnamed in where it went PublishedJan 4, 2017ClassClass IIIStatusOngoingWhereArizona, Colorado and Ohio
- Medicine recall Virt-Advance Prenatal/Postnatal Softgels, Prescription Folic Acid Containing Dietary Supplement cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert. Class IIIFDA’s classJan 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 4, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Extra-Virt Plus DHA Prenatal/Postnatal Softgel, Prescription Multivitamin/Mineral Dietary Supplement with… cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert. Class IIIFDA’s classJan 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 4, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Virt-Select Prenatal/Postnatal Softgels, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based… cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert. Class IIIFDA’s classJan 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 4, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert. Class IIIFDA’s classJan 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 4, 2017ClassClass IIIStatusTerminatedWhereNationwide
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.