Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sucralfate Tablets Recalled by Nostrum Laboratories, Inc. Due to CGMP Deviations: The recalling firm filed for Chapter...
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 Nostrum Laboratories, Inc. directly.
Affected Products
Sucralfate Tablets, USP 1 gram, packaged in a) 100-count bottles NDC 29033-0003-01, and b) 500-count bottles, NDC 29033-0003-05), Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120.
Quantity: 60,608 bottles
Why Was This Recalled?
CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Nostrum Laboratories, Inc.
Nostrum Laboratories, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report