Perrigo Company PLC recalls 180mg Allergy Fexofenadine tablets (30 count) made in Czech Republic due to impurity issues found during stability testing. No remedy specified in official notice.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo is recalling 180mg Allergy Fexofenadine tablets that failed stability testing for impurity A. This could mean the medication might not work properly or be unsafe over time, though the exact risk isn't specified in the recall.
The tablets failed stability testing for a specific impurity (impurity A) that could affect the medication's safety or effectiveness. This means the tablets might not work as intended or could pose health risks over time, though the exact danger level isn't detailed in the recall.
People who bought the 30-count 180mg Allergy Fexofenadine tablets from Amazon in the Czech Republic (lot #1BR0462, expiring 10/31/2022) are affected. Those with allergies to fexofenadine or who take this medication regularly are at higher risk.
Check for the 30-count 180mg Allergy Fexofenadine tablets with lot number 1BR0462, manufactured in the Czech Republic, and expiring 10/31/2022. These were sold on Amazon with UPC 3 70030 11466 5.
Look for the lot number 1BR0462 and expiration date 10/31/2022 on the packaging.
The recall states the tablets failed stability testing for impurity A, but does not specify if they are safe to use. The manufacturer has not provided a remedy, so it's recommended to check with a healthcare provider.
Perrigo recalled the tablets because stability testing showed the presence of impurity A, which could affect the medication's safety or effectiveness.
Check the lot number on the packaging; the recalled product has lot #1BR0462 and expires 10/31/2022, manufactured in the Czech Republic.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0330-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0330-2022 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.
