FDA Drugs recall ·
Ascorbic Acid Inj recall
This is an FDA Class I recall — the most serious type.
Read the official FDA notice ↗
Product
Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska Pharmaceuticals, 742 Evergreen Drive, Bennet, NE 68317
Why was it recalled?
Presence of Particulate Matter: Presence of glass particulates.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot #SP2400058, Exp 12/31/2024
Distribution
Nationwide in the USA
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0040-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.