Perrigo recalls 180mg fexofenadine tablets with impurity issues found in stability testing. Affected lots expire March 2022 or April 2022. Consumers should contact Perrigo for details.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo is recalling 180mg fexofenadine tablets due to impurities detected during stability testing. This could pose a risk to health if the tablets are taken as directed. The recall affects specific batches with expiration dates through April 2022.
The tablets failed stability testing for a specific impurity that could be harmful if taken as directed. This impurity was detected during testing but does not indicate immediate danger in normal use.
People who own or use the recalled fexofenadine tablets from Perrigo, specifically those with the 150-count bottles labeled with lot numbers 0GR0528 (expiring March 31, 2022), 0KR0473 (expiring April 30, 2022), or 0LR0369 (expiring June 30, 2022).
Check for the 150-count bottle labeled 'basic+care' or 'allergy' with 180mg fexofenadine hydrochloride. Look for lot numbers 0GR0528 (expiring March 31, 2022), 0KR0473 (expiring April 30, 2022), or 0LR0369 (expiring June 30, 2022).
Look for the lot numbers 0GR0528, 0KR0473, or 0LR0369 on the bottle to confirm if your tablets are affected.
The recall is due to impurities detected during stability testing, but the tablets are not considered unsafe for normal use. Consumers should check the lot numbers to see if they are affected.
The recall record does not specify a remedy, so contact Perrigo directly for instructions on what to do with the affected tablets.
Check the lot numbers on the bottle: 0GR0528 (expiring March 31, 2022), 0KR0473 (expiring April 30, 2022), or 0LR0369 (expiring June 30, 2022).
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0331-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0331-2022 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.
