PlainRecalls
FDA Drug Moderate Class II Ongoing

Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01

Reported: March 27, 2024 Initiated: March 12, 2024 #D-0392-2024

Product Description

Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01

Reason for Recall

The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.

Details

Units Affected
22,644 ampuls
Distribution
Nationwide within the United States
Location
Cherry Hill, NJ

Frequently Asked Questions

What product was recalled?
Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01. Recalled by Hikma Pharmaceuticals USA Inc.. Units affected: 22,644 ampuls.
Why was this product recalled?
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 27, 2024. Severity: Moderate. Recall number: D-0392-2024.