Medicines, 2018
Shortlist up to four to read them side by side.
1,426 medicine recalls FDA’s Enforcement Report published in 2018, 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 6, 2026.
1,426of 1,426 medicine recallsshown with your filters
The list
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Staple Remover Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline NICC Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Skin Staple Remover Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Straight Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline General Purpose Instrument Set, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Liberator Medical Supply Catheter Insertion Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Irrigation W/Piston SYR Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline IV Start Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medical Equipment Affiliates IV Start Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Debridement Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Skin Biopsy Pack-LF, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Incision and Drainage Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Pacemaker Implant Pack, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Hip Replacement, Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Incision Drainage Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Anesthesia Kit, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Incision and Drainage Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Professional Hospital Supply Suture Removal Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Pack Latex Safe, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Professional Hospital Supply Suture Removal Kit, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Skin Stapler RMVR, Tray Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Incision Drainage Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Abdominal Surgery II Pack-LF, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Suture Removal Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Medline Incision & Drainage Tray, Sterile, Single Use Only Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide, and Guam and Puerto Rico named
- Medicine recall Glenmark Mometasone Furoate Cream, USP, 0.1%, 45 g CGMP Deviations: Market complaints related to “gritty texture”. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets CGMP deviations. Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Ultane (sevoflurane), 250 mL, Inhalation Anesthetic Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage. Class IIIFDA’s classFeb 7, 2018in FDA’s Enforcement Report2 statesnamed in where it went PublishedFeb 7, 2018ClassClass IIIStatusTerminatedWhereMississippi and Ohio
- Medicine recall Atorvastatin Calcium Tablets 10 mg, a) 90 count and b) 500 count bottles Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability Class IIIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 7, 2018ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Atorvastatin Calcium Tablets 20 mg, a) 90 count and b) 500 count bottles Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability Class IIIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 7, 2018ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Atorvastatin Calcium Tablets 40 mg, 90 count bottles Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability Class IIIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 7, 2018ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Vecuronium bromide for Injection, 10 mg vials Failed impurities/ degradation specifications: Out-of-specification (OOS) result for USP related compound F at the 12 month stability test station. Class IIIFDA’s classFeb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 7, 2018ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Clopidogrel Tablets, USP 75 mg, 30-count bottles LABELING: LABEL MIX-UP. FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 7, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 7, 2018ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Black Ant capsules, 4600mg, 4-count blister pack, labeling is in foreign language Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction,… Class IIFDA’s classFeb 7, 2018in FDA’s Enforcement Report2 statesnamed in where it went PublishedFeb 7, 2018ClassClass IIStatusTerminatedWhereNew Jersey and New York
- Medicine recall Indian God Lotion Spray Bottle, labeling is in foreign language Marked Without An Approved NDA/ANDA: FDA analysis found this product to contain diethyl phthalate, an inactive ingredient in several modified release solid… Class IIIFDA’s classFeb 7, 2018in FDA’s Enforcement Report2 statesnamed in where it went PublishedFeb 7, 2018ClassClass IIIStatusTerminatedWhereNew Jersey and New York
- Medicine recall Miraculous Evil Root capsules, 1200 mg, 6-count bottle, labeling is in foreign language Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction,… FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 7, 2018in FDA’s Enforcement Report2 statesnamed in where it went PublishedFeb 7, 2018ClassClass IStatusTerminatedWhereNew Jersey and New York
- Medicine recall GERMANY BLACK GOLD tablets, 2800 mg, 8-count bottle, labeling is in foreign language Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction,… FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 7, 2018in FDA’s Enforcement Report2 statesnamed in where it went PublishedFeb 7, 2018ClassClass IStatusTerminatedWhereNew Jersey and New York
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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