PlainRecalls
FDA Drug Moderate Class II Completed

Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC: 38779-3097-00.

Reported: July 10, 2024 Initiated: June 26, 2024 #D-0570-2024

Product Description

Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC: 38779-3097-00.

Reason for Recall

CGMP Deviations and Presence of Particulate Matter: Glass

Details

Recalling Firm
Medisca Inc.
Units Affected
113 bottles
Distribution
Nationwide in the USA and Canada
Location
Irving, TX

Frequently Asked Questions

What product was recalled?
Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC: 38779-3097-00.. Recalled by Medisca Inc.. Units affected: 113 bottles.
Why was this product recalled?
CGMP Deviations and Presence of Particulate Matter: Glass
Which agency issued this recall?
This recall was issued by the FDA Drug on July 10, 2024. Severity: Moderate. Recall number: D-0570-2024.