Perrigo recalls 100-count fexofenadine hydrochloride tablets with impurities found during stability testing. Affected lots from Czech Republic production may pose health risks. Consumers should contact Perrigo for details.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo is recalling 100-count fexofenadine hydrochloride tablets that failed impurity tests during stability testing. This could mean the tablets contain harmful substances that might cause health issues if taken.
The tablets failed stability testing for impurity A, which means they may contain harmful substances that could affect health when taken. This issue was detected during quality control checks.
People who own or use the recalled Perrigo fexofenadine tablets made in the Czech Republic. Those with the specific lot numbers listed in the recall are most at risk.
Check for the product name 'Perrigo Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 100 count bottle' with lot numbers 0CR0510 (exp 09/30/21), 0GR0445 (exp 01/31/22), 0LR0361 (exp 04/30/22), or 1AR0558 (exp 07/31/22).
Look for the specific lot numbers listed in the recall to confirm if your tablets are affected.
The tablets failed stability testing for impurity A, which means they may contain harmful substances that could affect health when taken.
Check for the product name 'Perrigo Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 100 count bottle' with lot numbers 0CR0510 (exp 09/30/21), 0GR0445 (exp 01/31/22), 0LR0361 (exp 04/30/22), or 1AR0558 (exp 07/31/22).
The recall record does not specify a remedy, so contact Perrigo directly for instructions.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0346-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0346-2022 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.
