L. Perrigo recalls 180mg allergy tablets with impurities that could cause harm. Affected lots expired by Jan 2024. Consumers should check NDC codes and contact for details.
Failed Impurities/Degradation Specifications
L. Perrigo is recalling 180mg fexofenadine allergy tablets due to failed impurities and degradation specifications. This could lead to harmful substances in the medication. Consumers should check their product's NDC code and lot number to see if it's affected.
The tablets failed impurities and degradation specifications, meaning they may contain harmful substances that could cause adverse effects. This is a quality issue that could lead to unsafe medication levels.
People who purchased the recalled fexofenadine tablets from Target stores between specific dates. Those with allergies to fexofenadine or who take it regularly are at higher risk.
Check for NDC codes: 11673-617-22 (15-count), 11673-617-39 (30-count), 11673-617-01 (70-count), or 11673-617-47 (150-count). Look for specific lot numbers and expiration dates listed in the recall notice.
Identify your NDC code and lot number to see if your tablets are in the recalled batches.
The recall states the tablets failed impurities and degradation specifications, but does not specify if they are safe to use. Consumers should check if their product is in the recalled batches.
Check the NDC code on the packaging: 11673-617-22 (15-count), 11673-617-39 (30-count), 11673-617-01 (70-count), or 11673-617-47 (150-count). Also check the lot number and expiration date.
The recall does not specify a remedy, so consumers should check if their product is affected and contact L. Perrigo for further instructions.
We’ve drafted a message you can send L. Perrigo Company to request your refund or repair — edit it as you like.
Subject: Recall D-0910-2023 — L. Perrigo Company L. Perrigo Company Hello, I own a L. Perrigo Company that is covered by recall D-0910-2023 from L. Perrigo Company. 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.
