Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc. Due to Failed Dissolution Specifications: Out of specification for dissolution...
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 Akorn, Inc. directly.
Affected Products
SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION, USP,200 mg/ 40 mg per 5mL, CHERRY FLAVOR, 16 fl oz (473 mL) bottles (NDC 50383-0823-16), Rx only, HI-TECH PHARMACAL CO. INC, Amityville, NY 11701
Quantity: 27,648 bottles (16 fl. oz. each)
Why Was This Recalled?
Failed Dissolution Specifications: Out of specification for dissolution of sulfamethoxazole.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Akorn, Inc.
Akorn, Inc. has 176 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report