Perrigo Company PLC recalls Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets (180mg) due to failed impurity testing. Products sold in the US from 2022 with specific lot numbers may contain harmful impurities.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo Company PLC has recalled Rite Aid's Allergy Relief Fexofenadine Hydrochloride tablets (180mg) because stability testing found harmful impurities. This could pose a health risk if the tablets are taken as directed.
The tablets failed stability testing for a specific impurity (impurity A) that could be harmful if consumed. This impurity was detected during testing but the exact health risk isn't specified in the recall notice.
People who purchased the recalled Rite Aid Allergy Relief tablets in the US between 2022 and 2023, particularly those with allergies or sensitive health conditions.
Check for the product name 'Allergy Relief Fexofenadine Hydrochloride tablets, 24HR, 180mg' on the label. Look for lot numbers like 1BR0462 (expiring 10/31/2022) or 0GR0528 (expiring 3/31/2022).
Identify the product by checking the label for the specific lot number and expiration date listed in the recall notice.
The product failed stability testing for a specific impurity (impurity A) that could be harmful if consumed, but the exact health risk isn't specified in the recall notice.
The recall notice does not specify a remedy, so you should check with Rite Aid or the manufacturer for further instructions.
The recall notice states that the tablets may contain harmful impurities, but it does not specify the exact health risks or how severe they are.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0348-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0348-2022 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.
