Medisca recalls 500mg Budesonide powder due to glass particles from manufacturing. Affected lots 202323/G and 202323/H expire July 2026. Stop using immediately to avoid potential injury.
CGMP Deviations and Presence of Particulate Matter: Glass
Medisca is recalling 500mg Budesonide powder because it contains glass particles from manufacturing. This could cause injury if the powder is inhaled or ingested. Affected products have specific lot numbers and expire July 2026.
The powder contains glass particles due to manufacturing deviations. If inhaled or ingested, these particles could cause injury to the respiratory system or digestive tract. This is a serious hazard requiring immediate action.
People who own or use the recalled Budesonide powder for inhalation. Those with respiratory conditions may be at higher risk from potential inhalation of glass particles.
Check the product label for the lot numbers 202323/G or 202323/H. The product expires July 2026 and is a white to off-white, odorless crystalline powder.
Discard the recalled Budesonide powder product as it contains glass particles that could cause injury.
The product contains glass particles due to manufacturing deviations, which could cause injury if inhaled or ingested.
Lot numbers 202323/G and 202323/H.
The product expires July 31, 2026.
We’ve drafted a message you can send Medisca to request your refund or repair — edit it as you like.
Subject: Recall D-0570-2024 — Medisca Medisca Hello, I own a Medisca that is covered by recall D-0570-2024 from Medisca. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
