DOPAMINE HYDROCHLORIDE Dopamine HCl Inj., USP, 200 mg/5 mL (40 mg/mL), 5 mL Single-dose, 25 vials per t Recall 2026
DOPAMINE HYDROCHLORIDEIssued September 4, 2026
DOPAMINE HYDROCHLORIDE Dopamine 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. — recalled per FDA on 9/4/2026. Reason: Lack of Assurance of Sterility.
What to do about this recall
- Agency
- FDA
- Issued
- Sep 4, 2026
- Brand
- DOPAMINE HYDROCHLORIDE
- Distribution
- 1 states
- Lots affected
- 2
Steps to take for this recall
Stop using it
Take it out of rotation. Don't consume, wear, or operate.
Verify the match
Compare lot numbers, UPCs, and dates against your product.
Return or dispose
Follow the manufacturer's instructions to refund or safely dispose.
What's recalled
Dopamine 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.
Why it was recalled
Lack of Assurance of Sterility
Affected products & lot numbers2 lots called out
Affected Lot Numbers
Check your product label — do not use if your lot number appears below.
| Lot Number |
|---|
| Lot # NL5230 |
| Exp Date:10/2027 |
Where was it sold1 state
US Nationwide.
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Frequently asked questions
Is the DOPAMINE HYDROCHLORIDE recall still active?
Yes, this recall is currently active as of September 4, 2026. Do not use or consume the affected product.
What lot numbers are affected?
Affected lot numbers: Lot # NL5230, Exp Date:10/2027. Check the label on your product.
What should I do if I have the recalled DOPAMINE HYDROCHLORIDE?
Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.