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.
Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
Xpect is recalling extra strength pain relief tablets that may contain unstable salicylic acid. This could pose health risks if the tablets are taken as directed. Consumers should check their product lot numbers to see if they are affected.
The tablets failed stability tests, showing higher levels of salicylic acid than expected. Salicylic acid is a compound that can be harmful in high concentrations, potentially causing health issues if the tablets are taken as directed.
People who own or use Xpect PAIN AWAY Extra Strength tablets with the specific lot numbers listed in the recall notice. Those taking the tablets for pain relief are most at risk if the salicylic acid levels are unstable.
Check the product label for the lot number (e.g., K-9335, AK-9419) and expiration date. The recall covers specific lots from October 2023 through January 2024.
Look for the lot number on the product label, such as K-9335 or AK-9419.
Reach out to Xpect customer service to confirm if your specific lot number is affected.
The tablets failed stability tests, showing higher levels of salicylic acid than expected, which could pose health risks.
Check the product label for the lot number (e.g., K-9335, AK-9419) and expiration date. The recall covers specific lots from October 2023 through January 2024.
Contact Xpect customer service to confirm if your specific lot number is affected. They will provide guidance on next steps.
We’ve drafted a message you can send Xpect to request your refund or repair — edit it as you like.
Subject: Recall D-0076-2022 — Xpect Xpect Hello, I own a Xpect that is covered by recall D-0076-2022 from Xpect. 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.
