L. Perrigo recalls 180mg Fexofenadine tablets with failed impurities. Consumers should check NDC 69842-0914-39 and lot 2DV1925 for affected units.
Failed Impurities/Degradation Specifications
L. Perrigo is recalling allergy relief tablets that may contain impurities. This could pose a health risk if the tablets degrade over time.
The tablets failed impurities and degradation specifications, which could mean harmful substances formed during storage. This might affect safety if the tablets are used after their expiration date or under improper conditions.
People who bought the 180mg Fexofenadine tablets from CVS Pharmacy in the US. Those with allergies or sensitive health conditions may be at higher risk.
Check for NDC code 69842-0914-39 and lot number 2DV1925 on the packaging. The product was distributed by CVS Pharmacy in the US.
Look for NDC 69842-0914-39 and lot number 2DV1925 on the packaging.
The recall states the tablets may have failed impurities and degradation specifications, but no specific safety advice is given.
Check for NDC code 69842-0914-39 and lot number 2DV1925 on the packaging.
The recall record does not specify any action steps for consumers.
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-0903-2023 — L. Perrigo Company L. Perrigo Company Hello, I own a L. Perrigo Company that is covered by recall D-0903-2023 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.
