Is this recall still active?

The FDA lists the recall as terminated (closed 08/05/2025). FDA has determined the recall is complete and closed it.

Checked Oct 26, 2026

Class IDrug recallTerminated

Ascorbic Acid Inj. Solution recall

Recalled by Staska Pharmaceuticals, Inc. of Bennet, NE · FDA report 11/13/2024

Not an official recall notice and may be delayed. Confirm with the manufacturer or the agency.

Class: Class I; Most serious
Status: Terminated; Closed 08/05/2025
Recall started: 09/30/2024
Distribution: Nationwide

Reason for recall

Presence of Particulate Matter: Presence of glass particulates.

Class I: A reasonable chance that using or being exposed to the product will cause serious health problems or death.

Recalled product

Product: Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska Pharmaceuticals, 742 Evergreen Drive, Bennet, NE 68317
Lot and code info: Lot #SP2400058, Exp 12/31/2024
Quantity: 4773 vials
Recall number: D-0040-2025
Event ID: 95503
Initiated by: Voluntary: Firm initiated

Where it was distributed

Nationwide in the USA

Nationwide

Recall timeline

09/30/2024Firm started the recall
11/07/2024FDA classified it as Class I
11/13/2024Published in the FDA enforcement report
08/05/2025FDA closed (terminated) the recall

Frequently asked questions

Why was Ascorbic Acid Inj. Solution recalled?: Presence of Particulate Matter: Presence of glass particulates.
What does Class I mean?: Class I is FDA's most serious recall category: a reasonable chance that using or being exposed to the product will cause serious health problems or death.
Where was the recalled product sold?: Nationwide in the USA
Is this recall still active?: The FDA lists the recall as terminated (closed 08/05/2025). FDA has determined the recall is complete and closed it.

Source: U.S. Food and Drug Administration, openFDA enforcement report · Last updated 11/13/2024 · Do not rely on openFDA to make decisions regarding medical care

Recall at a glance

Class: Class I
Status: Terminated
Type: Drug
Reported: 11/13/2024

FDA enforcement report search

What recall classes mean

Class IMost serious: A reasonable chance that using or being exposed to the product will cause serious health problems or death.
Class IIModerate: Use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
Class IIILow risk: Use of or exposure to the product is not likely to cause adverse health consequences.

Classes are assigned by the FDA based on the health hazard.

If you have a recalled product

Stop using or eating it. Check the lot number, UPC or date code against the recall.
Return it to the store or follow the firm's instructions for a refund, repair or disposal.
For medicines, talk to your pharmacist or doctor before stopping a prescription.
Report problems to the FDA through MedWatch or to the CPSC at SaferProducts.gov.

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About this data

Recalls: Recall information comes from NHTSA, FDA, USDA, CPSC and other agencies. A product, vehicle or lot may be affected even if it is not listed here, and listings may be delayed. Check the official recall notice and contact the manufacturer or dealer to confirm whether your item is included.

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