Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Budesonide Recalled by Medisca Inc. Due to CGMP Deviations and Presence of Particulate Matter: Glass
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 Medisca Inc. directly.
Affected Products
Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC: 38779-3097-00.
Quantity: 113 bottles
Why Was This Recalled?
CGMP Deviations and Presence of Particulate Matter: Glass
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medisca Inc.
Medisca Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report