Clinical Innovations — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Clinical Innovations has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 19 Jul 2022. Clinical Innovations is categorized under Beverages based on their predominant recall history.
Recall activity over time for Clinical Innovations
How serious are Clinical Innovations recalls?
FDA recall classifications by severity
Full FDA recall history for Clinical Innovations
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 19 Jul 2022Official FDA Notice | Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product | Firm received complaints of leaking, black liquid, and black particulates in the product vials. | Class IITerminated |
| 19 Jul 2022Official FDA Notice | Sweetums 24% Sucrose Solution Preservative Free 15 mL cups VPSU15037288. Each box contains 288 cups. Product is aseptic | Firm received complaints of leaking cups, black liquid, and black particulates in the 24% Sucrose Solution. | Class IITerminated |
| 19 Jul 2022Official FDA Notice | Sweetums 24% sucrose solution preservative free. Vials containing 1ml or 2ml of 24% sucrose in purified water. Produc | Firm received complaints of leaking, black liquid, and black particulates in the product vials. | Class IITerminated |
Where have Clinical Innovations recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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