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Class I: serious health riskTerminated

Staska Pharmaceuticals Ascorbic Acid Inj Recall

Ascorbic Acid Inj

Staska Pharmaceuticals, Inc. · Bennet, NE

Risk level
Class I
Reported by FDA
Nov 13, 2024
Recall ID
D-0040-2025
Check your lot numberHow we source this data

Summary

Staska Pharmaceuticals recalled Ascorbic Acid Inj starting Sep 30, 2024. The FDA classified it as Class I (serious health risk) and published enforcement report D-0040-2025 on Nov 13, 2024. Reason: Presence of Particulate Matter: Presence of glass particulates. Status: Terminated.

Why it was recalled

Presence of Particulate Matter: Presence of glass particulates.

Product description

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

Lot numbers, UPCs & expiration codes

Lot #SP2400058, Exp 12/31/2024

Where it was sold

Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0040-2025
Classification
Class I
Status
Terminated
Recall initiated
Sep 30, 2024
FDA report date
Nov 13, 2024
Quantity
4773 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Staska Pharmaceuticals, Inc.

Original FDA data

Every field from FDA enforcement report D-0040-2025, exactly as published.

Show all FDA fields
City
Bennet
State
NE
Status
Terminated
Country
United States
Event ID
95503
Address
742 Evergreen Dr
Code information
Lot #SP2400058, Exp 12/31/2024
Postal code
68317-2365
Report date
Nov 13, 2024
Product type
Drugs
Recall number
D-0040-2025
Classification
Class I
Recalling firm
Staska Pharmaceuticals, Inc.
Product quantity
4773 vials
Termination date
Aug 5, 2025
Reason for recall
Presence of Particulate Matter: Presence of glass particulates.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska Pharmaceuticals, 742 Evergreen Drive, Bennet, NE 68317
Distribution pattern
Nationwide in the USA
Recall initiation date
Sep 30, 2024
Initial firm notification
Letter
Center classification date
Nov 7, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0040-2025, published Nov 13, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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