Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
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 QuVa Pharma, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0572-2020 — QuVa Pharma, Inc. QuVa Pharma, Inc. recalls fentaNYL 550 mcg/55 mL (10 mcg/mL) in 0.9% Sodium Chlor Hello, I own a QuVa Pharma, Inc. recalls fentaNYL 550 mcg/55 mL (10 mcg/mL) in 0.9% Sodium Chloride 55 mL Syringe Preservative Free, Rx, QuVA Pharma 1075 West that is covered by recall D-0572-2020 from QuVa Pharma, 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.
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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.
