Perrigo Company PLC recalls Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets (60mg, 24 count) made in Czech Republic with impurity issues. Consumers should check lot numbers and contact Rite Aid for details.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo Company PLC has recalled Rite Aid's 60mg fexofenadine allergy relief tablets due to impurity issues found during stability testing. This could pose a risk to health if the impurities are harmful, though the exact risk level isn't specified in the recall notice.
The tablets failed stability testing for a specific impurity (impurity A) that could be harmful if present in the product. This means the tablets might contain unsafe levels of impurities that could affect health, though the exact health risk isn't detailed in the recall notice.
People who purchased the Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets (60mg, 24 count) made in the Czech Republic between 2021 and 2022 are affected. Those with allergies or sensitive health conditions may be at higher risk.
Check for the product name 'Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets, 60mg, 24 count', lot numbers 0JE2487 (expiring 01/31/2022) or 0ME2515 (expiring 04/30/2022), and the manufacturer's label indicating Czech Republic origin.
Look for the lot numbers 0JE2487 (expiring 01/31/2022) or 0ME2515 (expiring 04/30/2022) on the packaging.
The tablets failed stability testing for impurity A, which could pose a health risk if present in unsafe levels.
Check for the lot numbers 0JE2487 (expiring 01/31/2022) or 0ME2515 (expiring 04/30/2022) on the packaging.
The recall notice does not specify a remedy, so contact Rite Aid directly for instructions.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0347-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0347-2022 from Perrigo. 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.
