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Lower risk Drug recall · FDA · Published August 7, 2020

Santa Cruz Biotechnology Hand Sanitizing Gel Recall: Subpotent Drug Risk

Santa Cruz Biotechnology recalls 3 fl oz antimicrobial hand sanitizer with subpotent drug levels. This product may not be effective against germs. Consumers should check lot numbers and contact the company for details.

🇺🇸 FDA recall #D-1557-2020DrugSanta Cruz Biotechnology ›
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Contact the company

Recalling firmSanta Cruz Biotechnology, Inc10410 Finnell St · Dallas, TX 75220-2443
✎ GovInfoNow plain-language explainer

Santa Cruz Biotechnology is recalling their 3-fluid ounce hand sanitizing gel because it contains subpotent drug levels. This means the product may not be effective at killing germs as intended. Read more at govinfonow.com/recall/36848-santa-cruz-biotechnology-hand-sanitizing-gel-recall-subpotent-drug-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/36848-santa-cruz-biotechnology-hand-sanitizing-gel-recall-subpotent-drug-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1557-2020

Cite this page

“Santa Cruz Biotechnology Hand Sanitizing Gel Recall: Subpotent Drug Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/36848-santa-cruz-biotechnology-hand-sanitizing-gel-recall-subpotent-drug-risk. Based on FDA recall #D-1557-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1557-2020%22&limit=1).

The FDA announced on August 7, 2020, that Santa Cruz Biotechnology, Inc. voluntarily recalled UltraCruz Hand Sanitizing Gel Antimicrobial due to subpotent drug risks. The recall affects 14,238 bottles distributed nationwide.

How to tell if you have it

  • Brand: Santa Cruz Biotechnology
  • Product: UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol)
  • Size: 3 Fluid Oz./89 mL bottles
  • Lot code: BF12530
  • Expiration date: 05/11/2022

The hazard

The product is classified as a subpotent drug. The FDA listed the hazard simply as "Subpotent drug" without reporting specific incidents or injuries in this record.

Context

GovInfoNow's records show other recent recalls of similar products include CoValence Laboratories Remedy Gel Hydrocortisone 1% Recall (2026-03-18), CoValence Laboratories Skin Rehab Gel Recall (2026-03-18), and Gasco Isopropyl Alcohol 70% Recall (2026-05-29).

How to tell if you have this one

Check for the product name 'UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol)' and the lot number BF12530, which expires May 11, 2022.

  • Brand
    Santa Cruz Biotechnology
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number BF12530 on the bottle, which expires May 11, 2022.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “U.S.A. Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Aug 7, 202012. FDA classified it Class II: Aug 28, 202023. Published in FDA’s Enforcement Report: Sep 9, 202034. FDA terminated the recall: Jun 14, 2021420202021
  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-1557-2020 (August 7, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1557-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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