Fresenius Kabi USA, LLC recalls Midazolam Injection, USP, Preservative Free, 2 mg / 2 mL (1 mg / mL), 24 X 2mL Prefilled single-use syringes per
Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection, USP, 2 mg / 2 ml, Containing Syringes of Ondansetron Injection, USP, 4 mg / 2 mL
Recall notice
Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection, USP, 2 mg / 2 ml, Containing Syringes of Ondansetron Injection, USP, 4 mg / 2 mL
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Source Page by GovInfoNow · govinfonow.com/recall/41117-fresenius-kabi-usa-llc-recalls-midazolam-injection-usp-preservative-free · Recall date October 27, 2017 · FDA enforcement record: FDA #D-0152-2018
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“Fresenius Kabi USA, LLC recalls Midazolam Injection, USP, Preservative Free, 2 mg / 2 mL (1 mg / mL), 24 X 2mL Prefilled single-use syringes per.” GovInfoNow, recall dated October 27, 2017. https://govinfonow.com/recall/41117-fresenius-kabi-usa-llc-recalls-midazolam-injection-usp-preservative-free. Based on FDA recall #D-0152-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0152-2018%22&limit=1).
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We’ve drafted a message you can send Fresenius Kabi USA, LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0152-2018 — Fresenius Kabi USA, LLC Fresenius Kabi USA, LLC recalls Midazolam Injection, USP, Preservative Free Hello, I own a Fresenius Kabi USA, LLC recalls Midazolam Injection, USP, Preservative Free, 2 mg / 2 mL (1 mg / mL), 24 X 2mL Prefilled single-use syringes per that is covered by recall D-0152-2018 from Fresenius Kabi USA, LLC. 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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Where this comes from
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.
- Official source: FDA Recall #D-0152-2018 (October 27, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0152-2018 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.