L. Perrigo recalls 180mg Allergy Relief tablets with failed impurities/degradation specs. Affected lots expire by 04/24. Stop using immediately.
Failed Impurities/Degradation Specifications
L. Perrigo is recalling 180mg Allergy Relief tablets that may contain impurities or degrade improperly. This could pose a health risk, so affected users should stop using the product immediately.
The tablets failed impurities and degradation specifications, meaning they could contain harmful substances or break down into unsafe compounds. This poses a risk of adverse health effects if taken.
All owners of the recalled 180mg Allergy Relief tablets in 30-count, 45-count, or 90-count cartons. People with allergies or sensitive reactions may be at higher risk.
Check for 30-count cartons (NDC 36800-691-39), 45-count cartons (NDC 36800-691-95), or 90-count cartons (NDC 36800-691-75). The affected lots have specific expiration dates: 01/24, 12/23, or 04/24.
Discard all affected tablets as they may contain harmful impurities or degrade improperly.
The tablets failed impurities and degradation specifications, meaning they could contain harmful substances or break down into unsafe compounds.
Affected lots include: 2FV1948, 2ER0285, 2ER0411 (expiring 01/24), 2CR0653 (expiring 12/23), and 2GR0331 (expiring 04/24).
Check for 30-count cartons (NDC 36800-691-39), 45-count cartons (NDC 36800-691-95), or 90-count cartons (NDC 36800-691-75) with the specific expiration dates mentioned.
We’ve drafted a message you can send L. Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0912-2023 — L. Perrigo L. Perrigo Hello, I own a L. Perrigo that is covered by recall D-0912-2023 from L. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
