Dobutamine recalls
The FDA has published 7 recalls involving Dobutamine since 2013. The latest was reported on 2 Jul 2025. Most were for sterility. Hospira has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls7since 2013
Last 12 months0reported
Class I114% of total
Ongoing1latest 2 Jul 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 14%Class II 6 86%Class III 0 0%
Why dobutamine is recalled
Companies
Brands
By year
Ongoing dobutamine recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | DOBUTamine Injection, USP, 250 mg recalled by PfizerDobutamine | Pfizer | Other | Nationwide |
All dobutamine recalls, newest first
7 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | DOBUTamine Injection, USP, 250 mg recalled by PfizerDobutamine | Pfizer | Other | Nationwide |
| Drug | CLASS II | Dobutamine, (a) 1080MG IN D5W, (b) 760MG IN D5W, ionotrop recalled | Sentara Infusion Services | Sterility | Nationwide |
| Drug | CLASS II | DOBUTamine Injection, USP 250 mg/ Vial, For IV Use Only recalled | Hospira | Particulate Matter | Nationwide |
| Drug | CLASS II | Dobutamine 2000 mcg/mL in a) D5W-, b) D5W-, c) D5W recalled | Baptist Health Medical Towers Pharmacy and Infusion Services | Sterility | AR |
| Drug | CLASS II | Dobutamine HCL in D5W, Packaged as a) 240MG in Homepumps recalled | Sentara Enterprises | Sterility | NC, VA |
| Drug | CLASS I | DOBUTamine Injection, USP, 250 mg per Single-dose Fliptop Vial recalledDobutamine | Hospira | Particulate Matter | Nationwide |
| Drug | CLASS II | DOBUTamine in 5% Dextrose Injection, USP, 250 mg Total, 1000 mcg/mL recalledDobutamine In Dextrose | Hospira | Sterility | Nationwide |
Should you stop taking Dobutamine?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.