Opalescence Treswhite Supreme Peach Patient Kit
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1271-2013.
Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1271-2013.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Ultradent Products, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1271-2013.
Ultradent Products, Inc.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Ultradent Products, Inc. Recall FAQ
Ultradent Products, Inc. is the subject of a food safety report: Opalescence Treswhite Supreme Peach Patient Kit. The notice was published on March 8, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 104 units are potentially affected.