Every recall we track for Ultra Seal Corporation — 66 in all — plus the complaints and injury reports the public filed about them.
Ultra Seal Corporation recalls Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamab: 2-tablet packets manufactured for First Aid Direct with cGMP deviations. No remedy specified in recall notice.
Ultra Seal Corporation recalls 2-count electrolyte tablets due to cGMP deviations. Affected lots AK9797 and AK9254 from Honeywell Safety Products USA. Consumers should contact for details.
Ultra Seal recalls CETAFEN cough and cold relief tablets due to cGMP deviations. Affected lots were manufactured for HARTHealth in Seattle, WA. Consumers should check product details and contact Ultra Seal for guidance.
Ultra Seal Corporation recalls REMfresh Advanced Ion-Powered Melatonin 5mg caplets due to cGMP deviations. Products with lot numbers 19B011, 19B012, 19B012A, 19E023 and expiration 05/2022 are affected.
Ultra Seal Corporation recalls phenylephrine nasal decongestant tablets due to cGMP deviations. Affected lots include AK985: 2-count packets, expiring 10/2022. No specific remedy stated in recall.
Ultra Seal recalls cold tablets with cGMP deviations. These products may have quality issues affecting safety.
Ultra Seal recalls 2-tablet pain reliever with acetaminophen, aspirin, caffeine and salicylamide due to cGMP deviations. No remedy specified in official notice.
Ultra Seal Corporation recalls 2-count AYPANAL acetaminophen tablets due to cGMP deviations. Consumers should contact Honeywell Safety Products for details.
Ultra Seal Corporation recalls Cold Relief Severe Pain/Cough products with cGMP deviations. Affected lots may contain unsafe levels of ingredients. Consumers should contact the company for details.
Ultra Seal Corporation recalls SINU-PHEN PLUS sinus pain and congestion tabs due to cGMP deviations. Affected products include 2-tablet packets with NDC 69103-2536-00, lot AK976: 08/2022 expiration.
Ultra Seal Corporation recalls Exaprin pain reliever tablets due to manufacturing quality issues. Affected lots were produced for HARTHealth in Seattle, WA with specific expiration date.
Ultra Seal Corporation recalls MAGNAC: calcium carbonate tablets due to manufacturing quality control issues. Affected lots produced for Afassco Inc. in Minden, NV. No specific remedy stated in recall notice.
Ultra Seal Corporation recalls 2-caplet packets of Extra Strength Unaspirin (acetaminophen 500mg) due to cGMP deviations. Affected lots expire May 2022 or June 2022. No remedy specified in official notice.
Ultra Seal Corporation recalls 100-count PEPTIME Energy caffeine tablets due to cGMP deviations. Consumers should check lot numbers 19E021 and 19E022 for affected products.
Ultra Seal recalls Extra Strength acetaminophen pain relievers with cGMP deviations. Affected lots may cause safety issues.
Ultra Seal Corporation recalls Sinus Relief (acetaminophen 325mg, guaifenesin 200mg, phenylephrine HCl 5mg) 2-tablet packets due to cGMP deviations. Affected lots expire 01/2022 or 06/2022.
Ultra Seal Corporation recalls Back Pain-Off tablets due to manufacturing quality deviations. Affected lots expired by July 2022. Consumers should check product labels for specific lot numbers and expiration dates.
Ultra Seal Corporation recalls Cystex Urinary Pan Relief tablets due to cGMP deviations. Affected lots expire by 2022. Consumers should check packaging for lot numbers and expiration dates.
Ultra Seal Corporation recalls mint-flavored antacid tablets due to cGMP deviations. Affected lots from March 2022 expire in June 2022. Consumers should check product labels for NDC 67060-303-68 and lot numbers AK9523 or AK9670.
Ultra Seal Corporation recalls Mint Flavor MIRAL: 2-count calcium carbonate tablets due to cGMP deviations. No specific remedy stated in official notice.
Ultra Seal recalls CETAFEN Extra Non-Aspirin Pain Relieve caplets due to cGMP deviations. These 2-count packets, manufactured for HARTHealth, may have quality issues.
Ultra Seal Corporation recalls DBI 357 Super Magnum Quick Energy Stimulant tablets due to cGMP deviations. Affected lots include 36-count, 100-count, and 500-count bottles with specific expiration dates.
Ultra Seal Corporation recalls Lite Remfresh Advanced Ion-Powered Melatonin 0.5mg tablets due to cGMP deviations. Affected lots expire May 2022. Consumers should check product details and contact Ultra Seal for guidance.
Ultra Seal Corporation recalls CONGESTAID II Nasal Decongestant (Phenylephrine HCl 5mg) 2 tablet packets due to cGMP deviations. Affected lots expire 02/2022 and 09/2022.
Ultra Seal Corporation recalls PAINAID 2-tablet packets due to cGMP deviations. Affected lots expired by January 2022 or August 2022. No remedy specified in official notice.
Ultra Seal Corporation recalls Nutralox Mint Antacid chewable tablets due to cGMP deviations. Affected lots from April 2022 expire May 2022. No specific remedy stated in official notice.
Ultra Seal Corporation recalls MidNite Sleep Health melatonin tablets due to cGMP deviations. Affected lots expire 02/2022 to 07/2022. Consumers should check labels for lot numbers and expiration dates.
Ultra Seal Corporation recalls PAINA: 2 caplet packets of premenstrual formula with acetaminophen 500mg and pamabrom 25mg due to cGMP deviations. No remedy specified in official notice.
Ultra Seal recalls cold/sinus pain reliever nasal decongestant due to cGMP deviations. Products contain acetaminophen 325mg and phenylephrine HCl 5mg. Check lot number K9708 from 07/2022.
Ultra Seal Corporation recalls Legatrin PM Pain Reliever/Sleep Aid (acetaminophen 500mg, diphenhydramine 50mcg) 50-count bottles due to cGMP deviations. Affected lots have specific expiration dates and NDC numbers.
Ultra Seal Corporation recalls CHLORESIN 2-tablet packets manufactured with cGMP deviations. Affected lots include AK9492 (expiring 02/2022).
Ultra Seal Corporation recalls Sinus Relief Headache/Nasal tablets due to cGMP deviations. Affected lots include AK9436 (expiring 01/2022).
Ultra Seal Corporation recalls Pain Away pain reliever due to cGMP deviations. Affected lots expired by Feb 2022. Consumers should contact manufacturer for details.
Ultra Seal Corporation recalls extra strength PAIN TERMINATOR pain relief tablets due to cGMP deviations. Affected lots manufactured in Palm Desert, CA. No specific remedy stated in recall notice.
Ultra Seal Corporation recalls headache and congestion relief tablets due to manufacturing quality issues. Affected products include specific lots from 2022 with NDC 42961-0206-02. Consumers should check labels for lot numbers and expiration dates.
Ultra Seal Corporation recalls PAPENOL (acetaminophen 500 mg) tablets due to cGMP deviations. Affected lots expired by February 2022.
Ultra Seal Corporation recalls 2-count cold relief tablets with cGMP deviations. Affected lots expired by July 2022. No remedy specified in official notice.
Ultra Seal Corporation recalls FEM-PRIN Menstrual Relief tablets due to cGMP deviations. Affected lots manufactured for HARTHealth in Seattle, WA. No specific remedy stated in official recall.
Ultra Seal Corporation recalls PEPTIME Energy caffeine tablets (350mg) due to cGMP deviations. Affected lots: 19E032 (6-count) and 19E033 (100-count).
Ultra Seal Corporation recalls DILOTAB II cold relief tablets due to cigarette manufacturing deviations. Affected lots expire by April 2022 and June 2022. Stop using immediately.
Ultra Seal Corporation recalls PEPTIME Energy caffeine tablets (250mg) due to cGMP deviations. Affected products include 6-count packets and 100-count bottles. No specific remedy is stated in the recall notice.
Ultra Seal Corporation recalls Cetafen non-aspirin pain relievers with acetaminophen 325mg due to cGMP deviations. Affected lots expired by June 2022.
Ultra Seal Corporation recalls nasal decongestant tablets with cGMP deviations. Affected lots expire 02/2022 or 09/2022. No remedy stated in official notice.
CVS Health recalls 30-count melatonin chewable tablets due to cGMP deviations. Consumers should check lot numbers on packaging for affected batches.
Ultra Seal Corporation recalls PAINAID BRF Back Relief Formula tablets due to cGMP deviations. This may affect safety standards for medication production.
Ultra Seal Corporation recalls Cold Relief (acetaminophen 250mg, guaifenesin 200mg, phenylephrine HCl 5mg) due to cGMP deviations. Products manufactured for First Aid in Mason, OH with specific lot numbers and expiration dates are affected.
Ultra Seal Corporation recalls Dolog: acetaminophen 325mg and dexbrompheniramine 1mg caplets in 90-count and 2-count packs due to cGMP deviations. No remedy specified.
Ultra Seal Corporation recalls Ephedrine Plus tablets due to manufacturing deviations. Check NDC 65193-320-24, lots 18M063 (exp 01/2022) and 19G076 (exp 09/2022).
Ultra Seal recalls Maximum Strength Non-Aspirin Pain Reliever (acetaminophen 50:000 mg) 2-tablet packets due to cGMP deviations. Consumers should check lot numbers and expiration dates.
REMfresh Advanced Ion-Powered Melatonin 2mg caplets with specific lot numbers recalled due to cGMP deviations. Consumers should contact the manufacturer for details.
Ultra Seal Corporation recalls AERO TAB Cold Relief 2-tablet packets due to manufacturing quality issues. This product contains acetaminophen, guaifenesin, and phenylephrine. Consumers should check lot numbers and contact the company for details.
Ultra Seal Corporation recalls PEPTIME Energy caffeine tablets (300mg) due to cGMP deviations. Affected lots 19E030 and 19E031 from 6-count packets and 100-count bottles.
Ultra Seal recalls COLD TERMINATOR cold relief tablets due to cGMP deviations. Affected lots manufactured in Carlsbad, CA with NDC 69103-2556. No remedy specified in official notice.
MidNite Natural sleep aid chewable tablets with melatonin 1.5mg are recalled due to cGMP deviations. Consumers should check lot numbers and expiration dates for affected batches.
Ultra Seal Corporation recalls Backache & Muscle Relief tablets due to cGMP deviations. Affected lots expired by 2022. Consumers should check product details and contact for remedy.
Ultra Seal recalls Pain & Sinus Reliever nasal decongestant due to cGMP deviations. This product contains acetaminophen 50:000mg and phenylephrine HCl 5mg per 2 tablets.
Ultra Seal Corporation recalls PainAway II pain relief tablets due to unstable salicylic acid levels. Affected lots expire by Oct 2021, Dec 2021, Feb 2022. Consumers should check packaging for lot numbers and contact Ultra Seal for details.
Xpect recalls extra strength pain relief tablets due to unstable salicylic acid content. Affected lots from Oct 2023 to Jan 2024 may cause health risks. Check your product details to determine if recalled.
