Estee Lauder Recalls DENBLAN Toothpaste Due to Stability Data Issues
Estee Lauder Inc is recalling 3,791 tubes of DENBLAN Anticavity Fluoride Toothpaste because stability data does not support the product's expiry date.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The FDA classified this as a Class III recall, which by definition is unlikely to cause adverse health consequences. The issue is related to stability data and expiry dates rather than an active contamination or defect causing harm.
Plain-English summary
Estee Lauder Inc is voluntarily recalling 3,791 tubes of DENBLAN Anticavity Fluoride Toothpaste, Whitening formula. The product is a 2.6 oz/75 mL tube containing sodium monofluorophosphate 0.76% and is distributed in a light green carton with UPC 8-82381-07901-7 and code D079-01-1000. The recall is being conducted because stability data does not support the product's expiry date.
The recall covers all lot codes and shipment dates for this specific product configuration. The product was distributed nationwide. The FDA has classified this recall as Class III, indicating that use of or exposure to the violative product is not likely to cause adverse health consequences.
Consumers who have this product should stop using it and contact Estee Lauder Inc for further instructions or a refund. No illnesses or injuries have been reported in connection with this recall.
The recalled product
- Product
- DENBLAN Anticavity Fluoride Toothpaste, Whitening formula, sodium monofluorophosphate 0.76%, 2.6 oz/75 mL tube, Laboratories Darphin, Dist, Paris France
- Manufacturer
- Estee Lauder Inc
- Category
- Drug — Dental Care
- Affected units
- 3,791
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- UPC: 8-82381-07901-7 Code: D079-01-1000
Distribution
Distributed nationwide across the United States.
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