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.
Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
Ultra Seal Corporation is recalling PainAway II pain relief tablets because they may contain unsafe levels of salicylic acid. This could lead to health risks if taken as directed. The recall affects specific production lots with expiration dates through February 2022.
The tablets may have unstable salicylic acid levels due to failed stability testing. This could lead to unexpected health effects if taken as directed, though the risk is not severe under normal use conditions.
People who own or use PainAway II tablets from the recalled lots (packaged in 12,000 per case) are affected. Those with sensitive health conditions or taking other medications may be at higher risk.
Check the packaging for lot numbers: AK-9336 (expires Oct 21, 2021), K9406/K9407 (expires Dec 21, 2021), K9860 (expires Oct 22, 2021), or AK-1057 (expires Feb 23, 2022). The product is sold in 12,000 tablets per case.
Look for lot numbers on the packaging: AK-9336, K9406, K9407, K9860, or AK-1057.
The tablets may contain unsafe levels of salicylic acid due to failed stability testing.
Check the packaging for lot numbers: AK-9336 (expires Oct 21, 2021), K9406/K9407 (expires Dec 21, 2021), K9860 (expires Oct 22, 2021), or AK-1057 (expires Feb 23, 2022).
The recall does not require immediate discontinuation; check the lot number and contact Ultra Seal if you have the affected product.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0070-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0070-2022 from Ultra Seal. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
