Defective container: empty inhaler and leakage observed through the inhaler valve due to partially missing bottom seat (gasket).
Defective container: empty inhaler and leakage observed through the inhaler valve due to partially missing bottom seat (gasket).
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Cipla USA, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0938-2023 — Cipla USA, Inc. Cipla USA, Inc. recalls Albuterol Sulfate Inhalation Aerosol, 90 mcg, 200 Metered I Hello, I own a Cipla USA, Inc. recalls Albuterol Sulfate Inhalation Aerosol, 90 mcg, 200 Metered Inhalation, net content 6.7 g canister packaged in a box, Rx that is covered by recall D-0938-2023 from Cipla USA, Inc.. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
