Perrigo recalls 60mg allergy tablets due to impurity issues found in stability testing. Affected lots from Czech Republic production.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo is recalling 60mg fexofenadine allergy tablets that tested positive for impurities. This could pose a health risk if the impurities are harmful when taken.
The tablets failed stability testing for a specific impurity. This means the medication might contain harmful substances that could cause health issues when taken.
People who bought the 100-count fexofenadine tablets made in the Czech Republic between 2021 and 2022 are affected. Those with allergies to antihistamines may be at higher risk.
Check for the 100-count bottle labeled 'basic+care, allergy Fexofenadine Hydrochloride Tablets, 60 mg'. Look for lot numbers 0CR0510 (expires 9/30/2021) or 0LR0361 (expires 4/30/2022).
Look for the lot numbers 0CR0510 (expires 9/30/2021) or 0LR0361 (expires 4/30/2022) on the packaging.
The tablets failed stability testing for a specific impurity, which could pose a health risk if taken.
The official recall notice does not specify a remedy or action for affected products.
The recall indicates potential impurities that could cause health issues, but the exact risk level is not clearly stated.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0332-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0332-2022 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.