US Drug Recall Register
Class I · High risk Terminated Initiated Sep 30, 2024 (2 years ago)

Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter: Presence of glass particulates.

What was recalled

Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska Pharmaceuticals, 742 Evergreen Drive, Bennet, NE 68317

Recalling firm
Staska Pharmaceuticals, Inc.
Origin
NE, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0040-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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