Clinical Innovations recalls Sweetums 24% sucrose solution vials (1ml/2ml) due to leaking and black particulates. Product used in NICU/hospitals only. Check UPCs for affected lots.
Firm received complaints of leaking, black liquid, and black particulates in the product vials.
Clinical Innovations is recalling Sweetums 24% sucrose solution vials (1ml or 2ml) that have been reported to leak and contain black liquid and particulates. These vials are used in hospitals and NICUs for controlled administration of sucrose to patients.
The product vials have been reported to leak and contain black liquid and particulates. This could potentially cause contamination or incorrect dosing if the vials are used in medical administration, though the product is only used in hospital settings with strict protocols.
Healthcare professionals and NICU staff who use these vials for medical administration. Patients receiving the product in hospital settings are at risk if the vials are defective.
Check for vials with UPCs: VPSU15031250 (2mL), VPSU15033250 (1mL), or VPSU15033250B (individually wrapped 1mL). These vials are used in hospitals and NICUs for controlled administration of sucrose.
Look for vials with UPCs VPSU15031250 (2mL), VPSU15033250 (1mL), or VPSU15033250B (individually wrapped 1mL).
The product has been reported to leak and contain black liquid and particulates, which could affect medical administration in hospitals and NICUs.
The product is only used in hospital settings with strict protocols. If you have the vials, check for leaks and particulates before use.
Check the UPC on the vial: VPSU15031250 (2mL), VPSU15033250 (1mL), or VPSU15033250B (individually wrapped 1mL).
We’ve drafted a message you can send Clinical Innovations to request your refund or repair — edit it as you like.
Subject: Recall F-1684-2022 — Clinical Innovations Clinical Innovations Hello, I own a Clinical Innovations that is covered by recall F-1684-2022 from Clinical Innovations. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
