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FDAFDA · Food and drugs·Recall number D-0456-2017

MIDAZOLAM INJECTION, USP, *25 mg/5 mL, (5 mg/ mL), 5 mL vials, 10 Vials per carton, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173 --- NDC 63323-412-05

Published February 8, 2017 · Recall initiated: December 16, 2016

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Failed Impurities/Degradation Specifications

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
MIDAZOLAM
Manufacturer
Fresenius Kabi USA, LLC
Distributor
Nationwide and Puerto Rico
UPC
0363323411183
Lot
Lot 6007327, exp. 01-2017; Lot 6007329, exp. 01-2017
Risk classification
Class II
Area (FDA)
drug
Country
United States

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