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Stop using now Drug recall · FDA · Published April 4, 2016

Better Braids Un-Braid Recall: Microbial Contamination Risk

Keystone Laboratories recalls Better Braids Un-Braid (salicylic acid) due to microbial contamination. Check lot 10AN5 and UPC 07059600430.

🇺🇸 FDA recall #D-0853-2016DrugBetter Braids ›
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Recalling firmKeystone Laboratories Inc1103 Kansas St · Memphis, TN 38106-1913
✎ GovInfoNow plain-language explainer

What happened, in plain English

Keystone Laboratories Inc is recalling Better Braids Un-Braid, a salicylic acid product packaged in 12 FL. OZ. (355 ml) bottles. The recall is due to failed Staphylococcus aureus tests indicating microbial contamination. No specific remedy or action steps are currently listed in the record. Read more at govinfonow.com/recall/43016-better-braids-un-braid-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/43016-better-braids-un-braid-recall-microbial-contamination-risk · Updated October 11, 2026 · FDA enforcement record: FDA #D-0853-2016

Cite this page

“Better Braids Un-Braid Recall: Microbial Contamination Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43016-better-braids-un-braid-recall-microbial-contamination-risk. Based on FDA recall #D-0853-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0853-2016%22&limit=1).

Why it’s dangerous

The product failed a Staphylococcus aureus test, indicating it is contaminated with bacteria that can cause infections. Using a non-sterile product contaminated with S. aureus on the skin or scalp can lead to serious health issues.

Who’s affected

Consumers who purchased Better Braids Un-Braid packaged in 12 FL. OZ. (355 ml) bottles distributed in the U.S., including Maryland and New Jersey, are affected. Individuals using this over-the-counter product on their skin or hair are at risk of exposure to microbial contamination.

How to tell if you have this one

Look for Better Braids Un-Braid (salicylic acid), also known as Le Demelant, packaged in 12 FL. OZ. (355 ml) bottles. Check for UPC 07059600430 and Lot # 10AN5 on the packaging.

  • Brand
    Better Braids
  • Product
    BETTER BRAIDS UN-BRAID (salicylic acid), Le Demelant, Packaged in 12 FL. OZ. (355 ml) Bottles, Over the Counter Only
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if your bottle matches the recalled lot number 10AN5 and UPC 07059600430.

  2. Stop Using Immediately

    Discontinue use of the product due to the risk of microbial contamination from failed S. aureus tests.

Where it went and when

Where it was distributed

Distributed in Maryland and New Jersey.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

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

States: Maryland, New Jersey.

Recall timeline

FDA terminated this recall 51 days after the firm started it.

1. Firm started the recall: Apr 4, 201612. FDA classified it Class II: May 16, 201623. Published in FDA’s Enforcement Report: May 25, 201634. FDA terminated the recall: May 25, 201642016
  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-0853-2016 (April 4, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0853-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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