Exact FDA event identifier

Event 64534

1 recalled-product record grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: March 08, 2013
Product types: Food
Classifications: Class III
Statuses: Terminated
Recalling firm wording: Ultradent Products, Inc.

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

Opalescence Treswhite Supreme Peach Patient Kit

F-1271-2013

Recall number: F-1271-2013
Initiated: March 08, 2013
Classification: Class III
Status: Terminated
Recalling firm: Ultradent Products, Inc.
Quantity: 104 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot B6LZS, Part number 5705

Distribution pattern

USA: AL, CA, GA, IL, IN, MA, MD, MI, NJ, OK, PA, SC, UT; 12 International distributors: Germany, China, France, Spain