Ultra Seal Corporation recalls ZEE+ painaid ESF Extra-Strength tablets due to potential instability in aspirin compounds. Affected lots expire April 2022 or December 2022. Consumers should check packaging for lot numbers.
Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
Ultra Seal Corporation is recalling ZEE+ painaid ESF Extra-Strength tablets because lab tests found unstable aspirin compounds. This could lead to inconsistent medication levels, but the recall does not mention serious injury risks.
The tablets contain aspirin, which can break down into salicylic acid. Lab tests showed this breakdown exceeded safe levels, potentially causing inconsistent medication strength. However, the recall does not indicate immediate health risks.
People who own or use ZEE+ painaid ESF Extra-Strength tablets with lot numbers AK-9547 (expiring April 2022) or AK-9941 (expiring December 2022) are affected. Those taking these tablets for pain relief are most at risk.
Check the packaging for lot numbers AK-9547 (expires April 2022) or AK-9941 (expires December 2022). The product comes in 50-count or 125-count packages.
Look for lot numbers AK-9547 (expires April 2022) or AK-9941 (expires December 2022) on the packaging.
The recall states the tablets may have unstable aspirin compounds, but does not mention immediate health risks. Use with caution.
Check the packaging for lot numbers AK-9547 (expires April 2022) or AK-9941 (expires December 2022).
The recall does not specify a remedy, so contact Ultra Seal Corporation for guidance.
We’ve drafted a message you can send ZEE+ to request your refund or repair — edit it as you like.
Subject: Recall D-0072-2022 — ZEE+ ZEE+ Hello, I own a ZEE+ that is covered by recall D-0072-2022 from ZEE+. 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.
