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LowClass IIITerminated

FDA Food recall · Reported April 3, 2013

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.

Recall #
F-1271-2013
Affected scope
104 units
Initiated
March 8, 2013
Compiled from official public sources by the editorial team.
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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..

Low
severity level
104 units
affected scope
Class III
classification
April 3, 2013
reported

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.

Recall Insight

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.

Household Products recalls over time

Where this recall sits in its category - 3,056 household products recalls on record

50100150200250 20052008201120142017202020232026 115
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

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

Product description

Opalescence Treswhite Supreme Peach Patient Kit

Reason for recall

Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05.

Recall Profile

Structured summary of the FDA Food recall record
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.

Scale of Impact

104 units units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units) -
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (F-1271-2013) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

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.

Frequently Asked Questions

What product was recalled?
Opalescence Treswhite Supreme Peach Patient Kit. Recalled by Ultradent Products, Inc.. Units affected: 104 units.
Why was this product recalled?
Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05.
Which agency issued this recall?
This recall was issued by the FDA Food on April 3, 2013. Severity: Low. Recall number: F-1271-2013.
Where was the recalled product distributed?
Distribution: USA: AL, CA, GA, IL, IN, MA, MD, MI, NJ, OK, PA, SC, UT; 12 International distributors: Germany, China, France, Spain.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-1271-2013) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

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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.