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Class II · ModerateActive recall

Infumorph 200

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: 052001, 052003, Exp. Date 11/2024; 023012, 023014, Exp. Date 08/2024
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byHikma Berkeley Heights, NJ 07922
Brand nameINFUMORPH 200
Generic nameMORPHINE SULFATE
Active ingredient(s)MORPHINE SULFATE
Distributed by / forHikma Pharmaceuticals USA Inc.
NDC0641-6039-01
Show the full FDA record
Full product labelInfumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01
Recalling firmHikma Pharmaceuticals USA Inc.
DistributionNationwide within the United States
Quantity22,644 ampuls
Recall initiated2024-03-12
Report date2024-03-27
Recall completed—
Recall numberD-0392-2024
ClassificationClass II
FDA statusOngoing
Origin on fileCherry Hill NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.