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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Prescription Drugs

Staska Ascorbic Acid Injection Solution Recalled for Glass Particles

Agency Publication Date: November 7, 2024
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Summary

Staska Pharmaceuticals is recalling 4,773 vials of Ascorbic Acid (Vitamin C) Injection Solution due to the presence of glass particles inside the vials. The recall affects 50mL single-use vials with a concentration of 25,000mg/50mL. Healthcare providers and medical offices should stop using these vials immediately to avoid serious health risks and contact the manufacturer to arrange for a return.

Risk

Injecting a solution containing glass fragments can lead to severe health consequences, including blood vessel blockages in the lungs or other organs, internal inflammation, and swelling at the injection site.

What You Should Do

  1. This recall affects Staska Pharmaceuticals Ascorbic Acid Injection Solution (25,000mg/50mL) sold in 50mL single-use vials.
  2. Check the vial label for lot number SP2400058 with an expiration date of 12/31/2024.
  3. Stop using the recalled product immediately. Contact Staska Pharmaceuticals at 1-888-801-1370 or your distributor to arrange for the return of any unused vials.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

📋Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Ascorbic Acid Injection Solution (25,000mg/50mL)by Staska Pharmaceuticals
Variants: 50mL single use vial, 500mg/mL concentration, Preservative Free, Non-corn
Lot Numbers:
SP2400058 (Exp 12/31/2024)

Compounded drug for IV use. Labeled for office use only. Manufactured on 07/12/2024.

Product Images

“Ascorbic Acid Inj. Solution 25,000mg/50ml (500mg/ml), Rx only, STASK Pharmaceuticals”

“Ascorbic Acid Inj. Solution 25,000mg/50ml (500mg/ml), Rx only, STASK Pharmaceuticals”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95503
Status: Resolved
Manufacturer: Staska Pharmaceuticals, Inc.
Sold By: Medical offices; Authorized distributors
Manufactured In: United States
Units Affected: 4773 vials
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.