Perrigo recalls 100-count 180mg fexofenadine tablets with impurities. Consumers should check NDC 45802-847-78 and lot 2DR0351 for affected units.
Failed Impurities/Degradation Specifications
Perrigo is recalling 100-count boxes of 180mg fexofenadine tablets that may contain impurities. This could pose a health risk if the tablets are taken as directed.
The tablets may contain impurities that could cause health issues when taken. This is a quality control issue that affects the safety of the medication.
People who own or use the recalled 180mg fexofenadine tablets. Those with allergies to fexofenadine or its ingredients are at higher risk.
Check for NDC 45802-847-78 and lot number 2DR0351 on the packaging. The product was distributed by Perrigo in Allegan, MI.
Look for NDC 45802-847-78 and lot number 2DR0351 on the packaging.
The recall states the tablets may contain impurities, but the official notice does not specify if they are safe to take.
Check for NDC 45802-847-78 and lot number 2DR0351 on the packaging.
The official notice does not provide a specific remedy for this recall.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0907-2023 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0907-2023 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.
