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Lower risk Drug recall · FDA · Published August 20, 2024

Elevate Oral Care Recalls Just Right 5000 Toothpaste Due to Labeling Error

Elevate Oral Care recalls Just Right 5000 toothpaste (Lot G073DC) due to a label mix-up. Check your product details and contact the company for more information.

🇺🇸 FDA recall #D-0658-2024DrugElevate Oral Care ›
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Contact the company

Recalling firmElevate Oral Care342 Pike Rd Ste 23 · West Palm Beach, FL 33411-3820
✎ GovInfoNow plain-language explainer

Elevate Oral Care is recalling Just Right 5000, 1.1% Sodium Fluoride toothpaste in Candy Apple Flavor because of a labeling error. The specific issue is described as a label mix-up involving the product's packaging or documentation. The recall affects units distributed nationwide to direct customers. Read more at govinfonow.com/recall/32561-elevate-oral-care-recalls-just-right-5000-toothpaste-due-to.

Source Summary by GovInfoNow · govinfonow.com/recall/32561-elevate-oral-care-recalls-just-right-5000-toothpaste-due-to · Updated October 9, 2026 · FDA enforcement record: FDA #D-0658-2024

Cite this page

“Elevate Oral Care Recalls Just Right 5000 Toothpaste Due to Labeling Error.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/32561-elevate-oral-care-recalls-just-right-5000-toothpaste-due-to. Based on FDA recall #D-0658-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0658-2024%22&limit=1).

The FDA announced on Aug. 20, 2024, that Elevate Oral Care is recalling Just Right 5000 toothpaste due to a labeling mix-up hazard. The recall affects products distributed nationwide.

How to tell if you have it

  • Brand: Elevate Oral Care
  • Product: Just Right 5000 Toothpaste
  • Flavor: Candy Apple
  • Concentration: 1.1% Sodium Fluoride
  • Size: Net Wt. 3.4oz (97g)
  • NDC: 57511-002-1
  • Lot Code: G073DC
  • Expiration Date: 3/31/2026

The hazard

The recall involves a labeling mix-up for Just Right 5000 toothpaste. The FDA classified this as a Class III recall.

Context

GovInfoNow's records show Elevate Oral Care has one other recall on record since June 4, 2026, involving Elevate Povi-One 10% Povidone-Iodine Oral Antiseptic for sub potency risk. Other recent recalls of similar products include American Regent Levocarnitine Injection Recall (April 16, 2026) and American Health Packaging Buprenorphine Tablets Recall (Aug. 19, 2026). ORL Kids Natural Toothpaste Recall occurred on Dec. 8, 2025, citing CGMP deviations in bubblegum flavor.

How to tell if you have this one

Check your toothpaste tube for the brand 'Just Right 5000', flavor 'Candy Apple', and net weight '3.4oz (97g)'. Verify the NDC number is 57511-002-1 and the Lot number is G073DC with an expiration date of 3/31/2026.

  • Brand
    Elevate Oral Care
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product Details

    Verify if your toothpaste matches the recalled lot number G073DC and expiration date 3/31/2026.

  2. Contact the Manufacturer

    Reach out to Elevate Oral Care, LLC for further instructions regarding the labeling error.

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: “120 direct customers, Nationwide US. No foreign, DOD/VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Aug 20, 202412. FDA classified it Class III: Sep 12, 202423. Published in FDA’s Enforcement Report: Sep 18, 202434. FDA terminated the recall: Aug 5, 2025420242025
  1. Firm started the recall
  2. FDA classified it Class III
  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-0658-2024 (August 20, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0658-2024 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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