Lack of Assurance of Sterility; potential exposure to non-sterile lubricant during the filling process
Lack of Assurance of Sterility; potential exposure to non-sterile lubricant during the filling process
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 Nephron Pharmaceuticals Corp. to request your refund or repair — edit it as you like.
Subject: Recall D-0010-2016 — Nephron Pharmaceuticals Corp. Nephron Pharmaceuticals Corp. recalls Ipratropium Bromide 0.5 mg and Hello, I own a Nephron Pharmaceuticals Corp. recalls Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution, packaged in 30x3 mL Sterile Unit-Dose Vials, that is covered by recall D-0010-2016 from Nephron Pharmaceuticals Corp.. 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.
