Severity
Low
FDA Food recall · Reported April 3, 2013
Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05.
Ultradent Products, Inc. recalled Opalescence Treswhite Supreme Peach Patient Kit - a low-severity action.
Opalescence Treswhite Supreme Peach Patient Kit was recalled by Ultradent Products, Inc. in April 3, 2013. Reason: Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05.. Check the official notice for the remedy. Verify recall #F-1271-2013 with the FDA Food before acting.
The recall
Ultradent Products, Inc. issued this low-severity FDA Food recall-Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05..
Sourced from official FDA Food enforcement records. Verify recall #F-1271-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1271-2013) was formally reported on April 3, 2013, with the manufacturer initiating the action on March 8, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Ultradent Products, Inc. is listed as the recalling firm, operating out of South Jordan, UT. Federal records list the affected scope as 104 units.
The documented reason for this recall is: Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05. Distribution data in the federal record shows the product reached: USA: AL, CA, GA, IL, IN, MA, MD, MI, NJ, OK, PA, SC, UT; 12 International distributors: Germany, China, France, Spain. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 3,056 household products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
104 units
Related Recalls
6
0 from same agency
Opalescence Treswhite Supreme Peach Patient Kit
Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-1271-2013 |
| Date reported | April 3, 2013 |
| Date initiated | March 8, 2013 |
| Recalling firm | Ultradent Products, Inc. |
| Firm location | South Jordan, UT |
| Affected scope | 104 units |
| Distribution | USA: AL, CA, GA, IL, IN, MA, MD, MI, NJ, OK, PA, SC, UT; 12 International distributors: Germany, China, France, Spain |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported April 3, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.