Ultra Seal Recalls
66 recalls on record · August 26, 2020 to February 9, 2022 · Drugs
Recalls by year
20
21
22
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls SINU-PHEN PLUS sinus pain and congestion tabs (acetaminophen 500 mg, Phenylephrine HCl 5.0 mg) 2 tablet packets, Manufac
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls PAIN TERMINATOR extra strength pain relief (aspirin 162 mg, acetaminophen 110 mg, Caffeine 32.4mg, Salicylamide 152 mg)
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg, Guaifenesin 200mg, 5.0 Phenylephrine HCl) 2 tablet packe
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Cold/Sinus Pain Reliever/Fever Reducer Nasal Decongestant (acetaminophen 325 mg, Phenylephrine HCl 5mg), 2 tablets per p
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Pain Away Pain Reliever/Fever Reducer (NSAID) (acetaminophen 110 mg, aspirin 162 mg, salicylamide 152mg, caffeine 32.4 m
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Headache & Congestion Sinus Relief (acetaminophen 250 mg, phenylephrine HCl 5 mg) 2 tablets per packet, Mfd. for First A
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Cold Relief (acetaminophen 250 mg, guaifenesin 200mg, phenylephrine HCl 5 mg) 2 tablets per packet, Mfd. for First Aid D
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Backache & Muscle Relief (acetaminophen 250 mg, magnesium salicylate-tetrahydrate 290mg, caffeine 50 mg) 2 tablets per p
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamabrom 25mg), 2- tablet packets, Mfd. for First Aid Direct, Mason,
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Cold Relief Severe Pain/Cough (acetaminophen 325mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, phenylephrine HCl 5mg)
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Lite Remfresh Advanced Ion-Powered Melatonin (Melatonin 0.5mg) Tablets, 36-count blisters, Physician's Seal LLC, Boca Ra
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Multi Symptom Cold Relief (acetaminophen 325 mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, Phenylephrine HCl 5mg) ta
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Cetafen Non-aspirin pain reliever (acetaminophen 325mg) tablets, 2-count packets, Manufactured for: HARTHealth Seattle,
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Back Pain-Off (caffeine 50mg, magnesium salicylate 290mg) Tablets 2-count packets, Mfd for MEDIQUE PRODUCTS, Fort Myers,
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls MidNite Sleep Health (melatonin 1.5 mg) tablets, 30-count bottles, Distributed by: Mylan Consumer Healthcare, Inc. Morga
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Dologen (acetaminophen 325 mg and dexbrompheniramine maleate 1mg) caplets, packaged in a) 90-count bottles, b) 2-count p
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Ephedrine Plus (Ephedrine HCl 25mg, Guaifenesin 200mg) tablets, 24-count bottles, Marketed by: DMD Pharmaceuticals A Div
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls DBI 357 Super Magnum Quick Energy Stimulant (caffeine 200mg) tablets, packaged in a) 36-count bottles, b) 100-count bott
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Cystex Urinary Pan Relief (NSAID) (methenamine 162mg, sodium salicylate 162.5mg tablets) packaged in a) 40-count blister
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Legatrin PM Pain Reliever/Sleep Aid (acetaminophen 500 mg, diphenhydramine HCl 50mg caplets) 50-count bottles, Manufactu
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Extra Strength (ES) PAIN RELIEVER (acetaminophen 500 mg) 2 tablet packets, Manufactured by Ultratab Laboratories, Inc.
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls CHLORESIN (acetaminophen 325mg, dextromethorphan HBr 15mg, Guaifenesin 200mg, Phenylephrine HCl 5mg) 2 tablet packets, M
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Maximum Strength Non Aspirin Pain Reliever/Fever Reducer (acetaminophen 500 mg) 2 tablet packets, Mfg. for: Advanced Fir
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls AERO TAB Cold Relief (acetaminophen 325 mg, Guaifenesin 200mg, Phenylephrine HCl 5mg) 2 tablet packets, Mfg. for: Aero H
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Cold Tablet Pain Reliever/Fever Reducer/Expectorant/Nasal Decongestant (acetaminophen 325 mg, Guaifenesin 200mg, Phenyle
Hazard: cGMP deviations
February 9, 2022DrugsFDA
Ultra Seal Corporation recalls Nasal & Sinus Decongestant (phenylephrine HCl 5mg) 2 tablets per packet, Mfd. for Cintas First Aid & Safety, Mason OH 45
Hazard: cGMP deviations
November 3, 2021DrugsFDA
Ultra Seal Corporation recalls Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 Tablets/
Hazard: Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
November 3, 2021DrugsFDA
Ultra Seal Corporation recalls Xpect First aid Extra Strength PAIN AWAY (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 Tablets/package
Hazard: Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
November 3, 2021DrugsFDA
Ultra Seal Corporation recalls Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets Per Packet, Packag
Hazard: Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
November 3, 2021DrugsFDA
Ultra Seal Corporation recalls North by Honeywell PAIN STOPPER EXTRA STRENGTH (Acetaminophen 250 mg, Aspirin 250 mg, Caffeine 65 mg) tablets, 2 tablets
Hazard: Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.