Fresenius Kabi USA, LLC recalls Vecuronium bromide for Injection, 10 mg vials, Rx only, Mfd. for: Fresenius Kabi, Lake Zurich, IL 60047, Made in India,
Fresenius Kabi recalls 10mg Vecuronium bromide vials (NDC 63323-781-10, Lot ZG603) due to impurities detected in stability testing. This medication is for injection only and requires immediate action.
Recall notice
Failed impurities/ degradation specifications: Out-of-specification (OOS) result for USP related compound F at the 12 month stability test station.
Contact the company & request your remedy
What happened, in plain English
Fresenius Kabi is recalling 10mg Vecuronium bromide injection vials because testing found impurities that could be harmful. This medication is used for medical procedures and must be handled carefully. Read more at govinfonow.com/recall/40929-fresenius-kabi-vecuronium-bromide-10mg-vials-recall-impurities-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/40929-fresenius-kabi-vecuronium-bromide-10mg-vials-recall-impurities-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0426-2018
Cite this page
“Fresenius Kabi Vecuronium Bromide 10mg Vials Recall: Impurities Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40929-fresenius-kabi-vecuronium-bromide-10mg-vials-recall-impurities-risk. Based on FDA recall #D-0426-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0426-2018%22&limit=1).
Why it’s dangerous
The vials failed stability testing, showing impurities that could be harmful when injected. This issue may cause adverse reactions in patients receiving the medication.
Who’s affected
Patients prescribed this medication by doctors and healthcare facilities using the recalled vials. Those with specific medical conditions requiring this drug are at higher risk.
How to tell if you have this one
Check for vials labeled 'Vecuronium bromide for Injection, 10 mg' with NDC code 63323-781-10 and lot number ZG603. The expiration date is November 2018.
- Brand
Fresenius Kabi- Category
Drug
What to do — step by step
Check Vial Details
Look for the NDC code 63323-781-10 and lot number ZG603 on the vial label.
Questions people ask
Is this medication safe to use?
The recall record states the vials failed stability testing and showed impurities, so they are not safe for use.
What should I do if I have this medication?
The recall record does not specify a remedy, so contact your healthcare provider for guidance.
How can I tell if I have the recalled vials?
Check for vials with NDC code 63323-781-10 and lot number ZG603, which expire November 2018.
Contact Fresenius Kabi
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0426-2018 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0426-2018 from Fresenius Kabi. 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-0426-2018 (January 16, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0426-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- 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.