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,…
- Recall date
- January 16, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0426-2018
- FDA classification
- Class III
- Brand / firm
- Fresenius Kabi USA, LLC
- Sold / distributed
- Nationwide USA
Why it was recalled
Failed impurities/ degradation specifications: Out-of-specification (OOS) result for USP related compound F at the 12 month stability test station.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Vecuronium bromide for Injection, 10 mg vials, Rx only, Mfd. for: Fresenius Kabi, Lake Zurich, IL 60047, Made in India, NDC 63323-781-10
Get recall alerts
Free email alert whenever Fresenius Kabi USA, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Fresenius Kabi USA, LLC