FDA recall record

Hikma Injectables USA Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection recall — FDA D-0480-2024

Labeling: Wrong Barcode

Class IIIclassification
D-0480-2024official record ID
May 8, 2024report date

Recall record at a glance

Official recordD-0480-2024
CategoryDrug Recalls
ClassificationClass III
FDA record statusCompleted
Recalling firmHikma Injectables USA Inc.
Report dateMay 8, 2024
Recall initiation dateApr 30, 2024
Quantity1,895 bags
LocationDayton, NJ, United States

Official 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

Why the product was recalled

Labeling: Wrong Barcode

Distribution information

Nationwide within the United States

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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