Cipla recalls 0.25mg/2mL Budesonide inhalation suspension due to lack of sterility assurance. Affected lots expire 01/2024. Stop using immediately if you have this prescription medication.
Lack of Assurance of Sterility
Cipla is recalling a specific prescription inhaler due to a lack of sterility assurance. This could lead to infections if the product is used. People with this prescription medication should stop using it immediately.
The product lacks proper sterility assurance, meaning it could be contaminated with bacteria or other pathogens. If inhaled, this could cause infections or other health issues. This is a serious risk for people using the medication as prescribed.
Prescription users of this specific Budesonide inhaler. Those with the recalled lot numbers (GA20080, GA20081, GA20094) and expiration date 01/2024 are most at risk.
Check for the product name: Budesonide Inhalation Suspension 0.25mg/2mL. Look for lot numbers GA20080, GA20081, or GA20094 with expiration date 01/2024.
Discard the product if you have the recalled lot numbers (GA20080, GA20081, GA20094) and expiration date 01/2024.
No, this product has a lack of sterility assurance and should not be used. It could cause infections if inhaled.
Lot numbers GA20080, GA20081, and GA20094 with expiration date 01/2024.
Check the product label for lot numbers GA20080, GA20081, or GA20094 and expiration date 01/2024.
We’ve drafted a message you can send Cipla to request your refund or repair — edit it as you like.
Subject: Recall D-1545-2022 — Cipla Cipla Hello, I own a Cipla that is covered by recall D-1545-2022 from Cipla. 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.
