US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Mar 12, 2024 (2 years ago)

Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What 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

Recalling firm
Hikma Pharmaceuticals USA Inc.
NDC code
0641-6039-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0392-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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