PlainRecalls
FDA Drug Low Class III Completed

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

Reported: May 8, 2024 Initiated: April 30, 2024 #D-0480-2024

Product Description

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

Details

Recalling Firm
Hikma Injectables USA Inc
Units Affected
1,895 bags
Distribution
Nationwide within the United States
Location
Dayton, NJ

Frequently Asked Questions

What product was recalled?
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. Recalled by Hikma Injectables USA Inc. Units affected: 1,895 bags.
Why was this product recalled?
Labeling: Wrong Barcode
Which agency issued this recall?
This recall was issued by the FDA Drug on May 8, 2024. Severity: Low. Recall number: D-0480-2024.