The Recall Registry
Recall data checked 7 hours ago

Home Prescription medicine Medisca Inc. — Budesonide, USP (Micronized),…

Food & drug recall · FDAJune 26, 2024Serious

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

Do not stop taking this without speaking to your pharmacist or doctor.

What’s wrong

CGMP Deviations and Presence of Particulate Matter: Glass

The Recall Registry rates this seriousFDA Class II: temporary or medically reversible health harm.

What to do

Check the lot numbers below against what you have. Do not stop taking a prescription medicine because of a recall without speaking to your pharmacist or doctor first — for many medicines stopping is more harmful than continuing, and they can tell you whether yours is affected and what to do about it.

Who to contact: Recalling firm: Medisca Inc.

The product

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

Details

Units affected
113 bottles
Recall date
June 26, 2024
Brand
Medisca Inc.
Model, lot or SKU numbers
Lot #s: 202323/G, 202323/H, Exp. 07/31/2026
Where it was distributed

Nationwide in the USA and Canada

The official notice

This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.

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

Read it on FDA

Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.

Filed under: Prescription medicine

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