Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PREVACID 24HR LANSOPRAZOLE 15MG CAP 14CT distributed to specific Family Recalled by Family Dollar Stores, Llc. Due to CGMP Deviations: product held outside appropriate storage temperature...
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 Family Dollar Stores, Llc. directly.
Affected Products
PREVACID 24HR LANSOPRAZOLE 15MG CAP 14CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Quantity: Unknown
Why Was This Recalled?
CGMP Deviations: product held outside appropriate storage temperature conditions.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Family Dollar Stores, Llc.
Family Dollar Stores, Llc. has 149 total recalls tracked by RecallDetector.
Related Recalls
Icosapent Ethyl Capsules Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed Tablet/Capsule specifications: Red dots inside capsule and...
Zydus Pharmaceuticals (USA) Inc · March 9, 2026
Product label: Temozolomide Capsules Recalled by Rising Pharma Holding, Inc. Due to Failed Impurities/Degradation Specifications: An out-of-specification result observed during...
Rising Pharma Holding, Inc. · March 3, 2026
Semaglutide Inj. Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Tirzepatide Inj Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Tirzepatide Inj Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report