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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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Medium RiskFDA Drug
Medications & Supplements/Topical Products

Santa Cruz Biotechnology, Inc: UltraCruz Hand Sanitizing Gel Recalled for Low Alcohol Content

Agency Publication Date: August 28, 2020
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Summary

Santa Cruz Biotechnology, Inc. is recalling approximately 14,238 bottles of UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol) because the product was found to be subpotent. This means the gel contains less than the required amount of active alcohol, which makes it less effective at killing germs and bacteria on the skin. The recall affects 3 fl. oz. (89 mL) bottles distributed nationwide across the United States. Consumers who have purchased this product should stop using it and contact their healthcare provider or pharmacist for guidance.

Risk

A subpotent hand sanitizer does not contain enough active ingredient to effectively kill pathogens, potentially leaving users unprotected against harmful bacteria and viruses. This could increase the risk of infection if the user relies on the product for proper hand hygiene.

What You Should Do

  1. Check your bottle of UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol) in the 3 Fluid Oz./89 mL size.
  2. Verify the lot information: this recall specifically affects Lot BF12530 with an expiration date of 05/11/2022.
  3. Contact your healthcare provider or pharmacist for guidance if you have concerns regarding the effectiveness of the product or potential infections.
  4. Return any unused product to the place of purchase for a full refund.
  5. Contact the manufacturer, Santa Cruz Biotechnology, Inc., for further instructions regarding this recall.
  6. For additional questions or to report a related issue, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Manufacturer-initiated voluntary recall for subpotency.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol) (3 Fluid Oz./89 mL)
Model:
Recall #: D-1557-2020
Lot Numbers:
BF12530 (Exp 05/11/2022)
Date Ranges: Exp 05/11/2022

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86197
Status: Resolved
Manufacturer: Santa Cruz Biotechnology, Inc
Sold By: Nationwide distributors
Manufactured In: United States
Units Affected: 14,238 bottles
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 ยท 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.