Presence of Particulate Matter: The firm initiated the recall due to visible presence of particulate matter.
Presence of Particulate Matter: The firm initiated the recall due to visible presence of particulate matter.
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 Cadence Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1432-2012 — Cadence Pharmaceuticals Cadence Pharmaceuticals recalls OFIRMEV (acetaminophen) injection, 1000 mg/ Hello, I own a Cadence Pharmaceuticals recalls OFIRMEV (acetaminophen) injection, 1000 mg/100 mL (10 mg/mL), 24-count Single Use 100 mL Vials per carton, Rx only, that is covered by recall D-1432-2012 from Cadence Pharmaceuticals. 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.
