Perrigo Company recalls 100-count 60mg Fexofenadine Hydrochloride tablets (12HR) with impurity issues found in stability testing. Consumers should check lot numbers on the bottle.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo is recalling 100-count 60mg Fexofenadine Hydrochloride tablets that failed stability testing for impurities. This could pose a risk if the tablets degrade over time, though the exact danger isn't specified in the recall.
The tablets failed stability testing for an impurity called 'A' that could be harmful if the medication degrades over time. This impurity was detected during testing but the specific health risk isn't detailed in the recall.
People who own the recalled 100-count 60mg Fexofenadine Hydrochloride tablets (12HR) from Perrigo. Those with allergies to fexofenadine or other antihistamines may be at higher risk.
Check the bottle for the lot number: 0GR0445 (expires 1/31/2022), 0LR0361 (expires 4/30/2022), or 1AR0558 (expires 7/31/2022). The product is a 100-count 60mg antihistamine tablet with a 12-hour duration.
Look for the lot numbers 0GR0445, 0LR0361, or 1AR0558 on the bottle to confirm if it's recalled.
The recall states the tablets failed stability testing for impurities, but the specific health risk isn't detailed. Consult a doctor if you have concerns.
Check the lot numbers on the bottle: 0GR0445 (expires 1/31/2022), 0LR0361 (expires 4/30/2022), or 1AR0558 (expires 7/31/2022).
The recall does not specify a remedy, so contact Perrigo directly for guidance.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0342-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0342-2022 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.
