Drug recall D-0152-2018
Product
Midazolam Injection, USP, Preservative Free, 2 mg / 2 mL (1 mg / mL), 24 X 2mL Prefilled single-use syringes per carton, Rx only, Fresenius Kabi Lake Zurich, IL 60047, NDC 76045-001-20
Reason for recall
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
Lots and codes
Lot: 6400048
Recall details
- Recalling firm
- Fresenius Kabi USA, LLC, Wilson, NC
- Quantity
- 203136 syringes
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 27, 2017
- Terminated
- October 5, 2020
Related products
- Midazolam – drug information
- NDC 76045-211 Midazolam · Midazolam Hydrochloride 2 mg/2mL · Fresenius Kabi USA, LLC
- NDC 76045-002 Midazolam · Midazolam Hydrochloride 5 mg/mL · Fresenius Kabi USA, LLC
- NDC 76045-003 Midazolam · Midazolam Hydrochloride 10 mg/2mL · Fresenius Kabi USA, LLC
- NDC 76045-001 Midazolam · Midazolam Hydrochloride 2 mg/2mL · Fresenius Kabi USA, LLC