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Lower risk Drug recall · FDA · Published March 6, 2017

Sensodyne Repair & Protect Whitening Recall: Foreign Substance

GSK recalls specific lots of Sensodyne Repair & Protect Whitening toothpaste due to foreign substance and off-flavor complaints.

🇺🇸 FDA recall #D-0624-2017DrugSensodyne ›
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Recalling firmGSK Consumer Healthcare184 Liberty Corner Rd Ste 200 · Warren, NJ 07059-6868
✎ GovInfoNow plain-language explainer

What happened, in plain English

Glaxo SmithKline Consumer Healthcare is recalling specific lots of Sensodyne Repair & Protect Whitening toothpaste because they may contain a foreign substance. The issue involves the presence of Patchouli oil, which results in an off flavor or scent for consumers. This recall affects approximately 56,840 cases distributed nationwide. Read more at govinfonow.com/recall/41858-sensodyne-repair-protect-whitening-recall-foreign-substance.

Source Summary by GovInfoNow · govinfonow.com/recall/41858-sensodyne-repair-protect-whitening-recall-foreign-substance · Updated October 11, 2026 · FDA enforcement record: FDA #D-0624-2017

Cite this page

“Sensodyne Repair & Protect Whitening Recall: Foreign Substance.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/41858-sensodyne-repair-protect-whitening-recall-foreign-substance. Based on FDA recall #D-0624-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0624-2017%22&limit=1).

Why it’s dangerous

The recalled toothpaste contains a low concentration of an additional flavoring ingredient, Patchouli oil. This causes complaints of an off flavor or scent, which is primarily a quality and sensory issue rather than a direct physical injury hazard in this context.

Who’s affected

Consumers who purchased Sensodyne Repair & Protect Whitening toothpaste (3.4 oz tubes) between the manufacturing dates corresponding to lots A6J231 through A6M231. The product was distributed nationwide.

How to tell if you have this one

Check the tube for the brand name Sensodyne Repair & Protect Whitening, stannous fluoride 0.45%, and a net weight of 3.4 oz. Look for the NDC 0135-0575-01 and UPC 3 10158 84060 2. Verify the lot code (A6J231, A6J261, A6K171, A6K241, or A6M231) and expiration date (08/2018, 09/2018, or 10/2018).

  • Brand
    Sensodyne
  • Product
    Sensodyne Repair & Protect Whitening, (stannous fluoride 0.45% (0.15% w/v fluoride ion)), Net Wt. 3.4 oz, Distributed
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if your toothpaste matches the lot codes and expiration dates listed in the recall record.

  2. Contact Manufacturer

    The recall record does not specify a return or refund procedure; contact Glaxo SmithKline Consumer Healthcare for further instructions.

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: “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 15 months after the firm started it.

1. Firm started the recall: Mar 6, 201712. FDA classified it Class II: Mar 30, 201723. Published in FDA’s Enforcement Report: Apr 5, 201734. FDA terminated the recall: May 31, 2018420172018
  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-0624-2017 (March 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0624-2017 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