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 Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint Microbial contamination of Non-sterile Products; presence of yeast and potential B. Class IIFDA’s classAug 30, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 30, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint Microbial contamination of Non-sterile Products; presence of yeast and potential B. Class IIFDA’s classAug 30, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 30, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl Microbial contamination of Non-sterile Products; presence of yeast and potential B. Class IIFDA’s classAug 30, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 30, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl Microbial contamination of Non-sterile Products; presence of yeast and potential B. Class IIFDA’s classAug 30, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 30, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz Microbial contamination of Non-sterile Products; presence of yeast and potential B. Class IIFDA’s classAug 30, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 30, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Phentermine HCL Capsules, USP 15 mg Failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature… Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine. FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IStatusTerminatedWhereNationwide
- Medicine recall D-ZINE Rapid Size and Strength capsules, 10mgs, 90 count bottle, Hardcore Formulations Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine. FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only Presence of particulate matter: Visible glass flakes identified as lamellae in some drug product vials. Class IIFDA’s classAug 23, 2017in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedAug 23, 2017ClassClass IIStatusTerminatedWherePuerto Rico
- Medicine recall Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: Product was tested by FDA and found to contain andarine and ostarine. FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL Unit Dose Cup, a) unit dose cup (NDC 50383-720-15), b)… Crystallization with subpotent out of specification assay results for chlorhexidine. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Halyard 24-Hour Oral Care Kit q2, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse Crystallization with subpotent out of specification assay results for chlorhexidine. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Halyard 24-Hour Oral Care Kit q4, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse Crystallization with subpotent out of specification assay results for chlorhexidine. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall 0.9% Sodium Chloride Injection, USP Presence of Particulate Matter; stainless steel Class IIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: FDA analysis found the product to tainted with undeclared anabolic… FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02 mg chewable and ferrous Fumarate 75 mg)… Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the package. FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Voriconazole Tablets, 200 mg, 20-count cartons Failed impurities/degradation specifications: Out of specification for a related compound C. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Entecavir Tablets 0.5 mg, 30 tablets per container Failed Impurities/Degradation Specification: single unknown impurity OOS 0.33% (Limit:NMT 0.20%W/W) at the three month stability point. Class IIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNew Jerseythe one state its words name PublishedAug 23, 2017ClassClass IIStatusTerminatedWhereNew Jersey
- Medicine recall Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g Marketed without an Approved NDA/ANDA: The product consists of pure, powdered caffeine and is an unapproved drug due to stimulant claims. Class IIFDA’s classAug 23, 2017in FDA’s Enforcement Report3 statesnamed in where it went PublishedAug 23, 2017ClassClass IIStatusTerminatedWhereKentucky, Michigan and Virginia
- Medicine recall Beautipharm All Day Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl methoxycinnamide 4%) Facial Cream,… Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Beautipharm Body Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl methoxycinnamide 4%) Body Lotion, 8.3 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Beautipharm Eye Care Balm SPF 10 (Octocrylene 4% and Octyl methoxycinnamide 4%) Eye cream, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Transparent ivory (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Transparent pastel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Transparent sand (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Perfect caramel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Transparent dark tan (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Transparent terra (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Perfect ivory (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Perfect pastel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Perfect sand (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Perfect dark tan (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Make Up Perfect terra (Titanium Dioxide) SPF 10 liquid make-up, 1 oz Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. Class IIIFDA’s classAug 23, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 23, 2017ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Glipizide Extended-Release Tablets (anti-diabetic agent), 5 mg Failed Moisture Limits: out of specification test results for water content obtained during stability testing. Class IIIFDA’s classAug 16, 2017in FDA’s Enforcement Report6 statesnamed in where it went PublishedAug 16, 2017ClassClass IIIStatusTerminatedWhereConnecticut, Illinois, Michigan, Ohio, Pennsylvania and Virginia
- Medicine recall Nystatin Topical Powder, USP, 100,000 USP units per gram, 15 grams per bottle Presence of Foreign Substance: potential presence of plastic particles. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Oxygen Refrigerated Liquid USP UN 1073 GMP Deviations: The firm does not include an SOP for testing for out of specifications. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNew Jerseythe one state its words name PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNew Jersey
- Medicine recall Ephedrine Sulfate Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Ephedrine Sulfate Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Ephedrine Sulfate Injection Solution 1 mL, 50 mg/1 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Ephedrine Sulfate Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Glycopyrrolate Injection Solution, 5 mL 1 mg/5 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Glycopyrrolate Injection Solution, 2 mL 0.4 mg/2 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Glycopyrrolate Injection Solution, 1 mL 0.2 mg/1 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Succinylcholine Chloride Injection Solution 10 mL, 200 mg/10 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Succinylcholine Chloride Injection Solution 5 mL, 100 mg/5 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Norepinephrine Bitartrate 16 mg Added to 0.9% Sodium Chloride 250 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Norepinephrine Bitartrate 4 mg Added to 0.9% Sodium Chloride 250 mL Lack of Sterility Assurance. Class IIFDA’s classAug 16, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 16, 2017ClassClass 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.”
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