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Stop using now Drug recall · FDA · Published February 8, 2016

Recall: Medicated Better Braids La Laque Spray Due to Contamination

Keystone Laboratories recalls Lot 9AD5 of La Laque spray due to Staphylococcus aureus contamination. Check your bottle and stop use immediately.

🇺🇸 FDA recall #D-0726-2016DrugMedicated Better 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 has recalled one lot of Medicated Better Braids, La Laque (salicylic acid) Spray because it tested positive for Staphylococcus aureus. This microbial contamination means the non-sterile product is unsafe for its intended use on hair and scalp. The recall covers 134 cases distributed nationwide and in Canada. Read more at govinfonow.com/recall/43166-recall-medicated-better-braids-la-laque-spray-due-to-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/43166-recall-medicated-better-braids-la-laque-spray-due-to-contamination · Updated October 11, 2026 · FDA enforcement record: FDA #D-0726-2016

Cite this page

“Recall: Medicated Better Braids La Laque Spray Due to Contamination.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43166-recall-medicated-better-braids-la-laque-spray-due-to-contamination. Based on FDA recall #D-0726-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0726-2016%22&limit=1).

Why it’s dangerous

The product contained Staphylococcus aureus, a bacterium that can cause infections. Because the spray is non-sterile and intended for topical use, applying it could introduce this pathogen to the skin or hair follicles, potentially leading to infection.

Who’s affected

Consumers who purchased Medicated Better Braids, La Laque spray from retailers across the United States and Canada are affected. Individuals using this product on their hair or scalp are at risk of exposure to harmful bacteria.

How to tell if you have this one

Check your bottle for the label 'Medicated Better Braids, La Laque (salicylic acid) Spray, 2%, 12 Fl. OZ. (355 ml.)'. Verify the Lot Number is 9AD5 and the UPC is 0 70596 00422 5.

  • Brand
    Medicated Better Braids
  • Product
    Medicated Better Braids, La Laque (salicylic acid) Spray, 2%,12 Fl. OZ. (355 ml.) bottle, Distributed by Keystone
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not use the spray if it matches the recalled lot number, as it contains harmful bacteria.

  2. Discard or return the item

    The record does not specify a return address or refund process; consumers should dispose of the product safely.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

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: “Nationwide and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: Feb 8, 201612. FDA classified it Class II: Feb 22, 201623. Published in FDA’s Enforcement Report: Mar 2, 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-0726-2016 (February 8, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0726-2016 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