Perrigo recalls Meijer allergy relief tablets with potential impurities. Affected lots from 2021-2022 may contain harmful substances. Consumers should check NDC codes and contact Meijer for details.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo Company PLC is recalling Meijer allergy relief tablets that may contain harmful impurities. This could pose a health risk if the tablets are taken as directed. Affected products include 15-count, 30-count, and 45-count bottles with specific lot numbers and expiration dates.
The tablets failed stability testing for a specific impurity. This means the medication may contain harmful substances that could affect health if taken as intended. The issue was detected during quality control checks.
Meijer pharmacy customers who purchased the recalled allergy relief tablets between 2021 and 2022. People taking the medication for allergies are most at risk if they have the affected lots.
Check for the product name 'Meijer allergy relief', 24HR, 1800mg antihistamine tablets. Look for NDC codes 41250-060-22, 41250-060-39, or 41250-060-95. The products were made in the Czech Republic and distributed by Meijer.
Identify the NDC code and expiration date on the packaging to confirm if your product is affected.
The tablets failed stability testing for a specific impurity, which could pose a health risk if taken as directed.
The official recall notice does not specify a remedy or action for affected products.
Affected lots include 0HE2530 (exp 12/31/2021), 0KE2430 (exp 2/28/2022), 0LR0362 (exp 6/30/2022), 1BR0462 (exp 10/31/2022), and 0FR0460 (exp 2/28/2022).
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0343-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0343-2022 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.
