Dextrose Monohydrate recalls
The FDA has published 14 recalls involving Dextrose Monohydrate since 2013. The latest was reported on 15 Apr 2026. Most were for sterility. Baxter Healthcare 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 recalls14since 2013
Last 12 months3reported
Class I536% of total
Ongoing4latest 15 Apr 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 5 36%Class II 9 64%Class III 0 0%
Why dextrose monohydrate is recalled
Companies
By year
Ongoing dextrose monohydrate recalls
4 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | 5% Dextrose Injection, USP per (50 mg per mL) in a freeflex recalledDextrose | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 5% Dextrose Injection, USP per (50 mg per mL) in a freeflex recalledDextrose | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 5% Dextrose Injection, USP per (50 mg per mL) in a freeflex recalledDextrose | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS I | Infant 25% Dextrose Injection recalled by HospiraDextrose | Hospira | Particulate Matter | Nationwide |
All dextrose monohydrate recalls, newest first
14 totalShould you stop taking Dextrose Monohydrate?
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.