FDA Drug Critical Class I Terminated

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

Reported: November 13, 2024 Initiated: September 30, 2024 #D-0040-2025

Product Description

Reason for Recall

Presence of Particulate Matter: Presence of glass particulates.

Details

Recalling Firm: Staska Pharmaceuticals, Inc.
Units Affected: 4773 vials
Distribution: Nationwide in the USA
Location: Bennet, NE

Frequently Asked Questions

What product 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. Recalled by Staska Pharmaceuticals, Inc.. Units affected: 4773 vials.

Why was this product recalled? ▼

Presence of Particulate Matter: Presence of glass particulates.

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on November 13, 2024. Severity: Critical. Recall number: D-0040-2025.

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