Presence of Particulate Matter: particles identified as polydimethylsiloxane (PDMS)
Presence of Particulate Matter: particles identified as polydimethylsiloxane (PDMS)
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 Hikma Pharmaceuticals USA INC to request your refund or repair — edit it as you like.
Subject: Recall D-0864-2020 — Hikma Pharmaceuticals USA INC Hikma Pharmaceuticals USA Inc. recalls Ketorolac Tromethamine Injecti Hello, I own a Hikma Pharmaceuticals USA Inc. recalls Ketorolac Tromethamine Injection, USP 30 mg/mL, packaged in 1 mL Single Dose Vials (NDC 0641-6042-01), 25 that is covered by recall D-0864-2020 from Hikma Pharmaceuticals 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.
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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.
