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Lower risk Drug recall · FDA · Published November 17, 2021

ASP CARES Ascorbic Acid Solution Recall: Lack of Sterility Risk

ASP CARES recalls 500 mg/mL Ascorbic Acid Solution for Injection vials due to lack of assurance of sterility. This could lead to infections if used improperly.

🇺🇸 FDA recall #D-0262-2022DrugASP CARES ›
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Recalling firmASP CARES2414 Babcock Rd Ste 106 · San Antonio, TX 78229-4870
✎ GovInfoNow plain-language explainer

What happened, in plain English

ASP CARES is recalling ascorbic acid injection vials because they may not be sterile. Using these vials could cause infections, especially in medical settings. Read more at govinfonow.com/recall/35530-asp-cares-ascorbic-acid-solution-recall-lack-of-sterility-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35530-asp-cares-ascorbic-acid-solution-recall-lack-of-sterility-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0262-2022

Cite this page

“ASP CARES Ascorbic Acid Solution Recall: Lack of Sterility Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35530-asp-cares-ascorbic-acid-solution-recall-lack-of-sterility-risk. Based on FDA recall #D-0262-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0262-2022%22&limit=1).

Why it’s dangerous

The vials may not be sterile, which can lead to infections if used for injections. This is a risk in medical settings where sterile solutions are critical.

Who’s affected

Healthcare professionals and patients who have been prescribed this medication. Those using the vials for injections are at risk of infection.

How to tell if you have this one

Check for the NDC code 72833-690-50 on the vial. The vials were manufactured in lots 092321690 and 093021690 with expiration dates of March 22, 2022 and March 29, 2022.

  • Brand
    ASP CARES
  • Category
    Drug
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    United States
Recall numberProduct, codes & lotsQuantity
D-0260-2022Methylcobalamin Solution for Injection, 1 mg/mL, 30 mL Multiple Dose Vial, For IM, SC or IV Use Only, Rx only, ASP Cares2414 Babcock Rd Ste #106, San Antonio, TX 78229 NDC 72833-565-30; Lot: 082921565 BUD: 02/25/20221605 vials
D-0261-2022Biotin Solution for Injection, 10 mg/mL, 30 mL Multiple Dose Vial, Sterile, For IM or IV use only, Rx only ASP Cares, 2414 Babcock Rd Ste #106, San Antonio, TX 78229 NDC 72833-0589-30; Lot: 091721589 BUD: 03/16/2022896 vials
D-0262-2022Ascorbic Acid Solution for Injection, 500 mg/mL, 50 mL Multiple Dose Vial, For IM, IV or SC Use Only, Rx only, ASP Cares, 2414 Babcock Rd Ste #106, San Antonio, TX 78229 NDC 72833-690-50; Lots: 092321690 BUD: 03/22/2022; 093021690 BUD: 03/29/20223077 vials
Based on the official FDA remedy

What to do — step by step

  1. Check Vial Expiration

    Verify the expiration date on the vial label; these vials expire by March 22, 2022 or March 29, 2022.

How this recall unfolded

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Nov 17, 202112. FDA classified it Class II: Nov 26, 202123. Published in FDA’s Enforcement Report: Dec 8, 202134. FDA terminated the recall: Dec 2, 2022420212022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0262-2022 (November 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0262-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA