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Class II · ModerateActive recall

Dopamine Hydrochloride

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

Does this affect you?
Check your lot numberLot # NL5230, Exp Date:10/2027
Where it was soldUS Nationwide.
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

Lack of Assurance of Sterility

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 byHospira, Inc.
Brand nameDOPAMINE HYDROCHLORIDE
Generic nameDOPAMINE HYDROCHLORIDE
Active ingredient(s)DOPAMINE HYDROCHLORIDE
Distributed by / forHospira, Inc., Lake Forest, IL 60045 USA, Vial
NDC0409-5820-11
Show the full FDA record
Full product labelDopamine HCl Inj., USP, 200 mg/5 mL (40 mg/mL), 5 mL Single-dose, 25 vials per tray, Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA, Vial NDC 0409-5820-11, Carton NDC 0409-5820-01.
Recalling firmPfizer
DistributionUS Nationwide.
QuantityN/A
Recall initiated2026-09-04
Report date2026-09-23
Recall completed—
Recall numberD-0853-2026
ClassificationClass II
FDA statusOngoing
Origin on fileManhattan NY United States

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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.