FDA recall D-0480-2024

Hikma Injectables USA Inc · Class III · drug

Product

Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection, packaged in 100mL bags, Rx only, Compounded by: Hikma Injectables USA Inc. 2 Esterbrook Lane, Cherry Hill, NJ 08003, Distributed by: Hikma Injectables USA Inc. 36 Stults Road, Dayton, NJ 08810, NDC 63037-100-05

Reason for recall

Labeling: Wrong Barcode

Distribution

Nationwide within the United States

Key facts

Status
Completed
Initiation date
2024-04-30
Report date
2024-05-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Dayton, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0480-2024