FDAClass INovember 13, 2024

Ascorbic Acid Inj. Solution recall: Particulate Matter

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 Ascorbic Acid Inj. Solution recalled?

Presence of Particulate Matter: Presence of glass particulates.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #SP2400058, Exp 12/31/2024

Product
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.
Quantity
4773 vials
Distribution
Nationwide in the USA
Recall date
November 13, 2024
Classification
Class I
Status
Terminated
Agency
FDA (drug)
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