Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in…
Recalling firm: Clinical Innovations, LLC
Firm received complaints of leaking, black liquid, and black particulates in the product vials.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 20, 2023.
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FDA code information
VPSU15032250 21029a 03/31/2023 VPSU15032250 21031a 03/31/2023
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Full FDA record and distribution details
Original product description
Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital setting including the NICU. -VPSU15032250, 1mL vial, bagged qty 250
Original FDA recall reason
Firm received complaints of leaking, black liquid, and black particulates in the product vials.
Recall details
- Recall number
- F-1685-2022
- Event ID
- 90607
- FDA status
- Terminated
- Initiated
- Jul 19, 2022
- Reported
- Sep 7, 2022
- Classified
- Sep 1, 2022
- Terminated
- Mar 20, 2023
- Quantity
- 10,922 boxes (250 vials/box) total
- Location
- Murray, UT, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
Nationwide - all 48 states plus Washington DC and Puerto Rico. Australia and United Arab Emirates (Dubai).
Data updated September 16, 2026. View official FDA data ↗
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