Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets Recalled by Perrigo Company PLC Due to Failed Impurities/Degradation Specifications; Out of specification result obtained...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Perrigo Company PLC directly.
Affected Products
Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, packaged as a) 30 count bottle, NDC 11822-0571-2 UPC 0 11822 99908 3; b) 150 count bottle, NDC 11822-0571-5 UPC 0 11822 85411 5; Made in the Czech Republic, Distributed by Rite Aid 30 Hunter Lane Camp Hill PA 17011
Quantity: 44,688 containers
Why Was This Recalled?
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Perrigo Company PLC
Perrigo Company PLC has 106 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report