FDAFDA · Food and drugs·Recall number D-0570-2024
Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC: 38779-3097-00.
Published July 10, 2024 · Recall initiated: June 26, 2024
Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations and Presence of Particulate Matter: Glass
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medisca Inc.
- Distributor
- Nationwide in the USA and Canada
- Lot
- Lot #s: 202323/G, 202323/H, Exp. 07/31/2026
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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