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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 76271

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

Open FDA event record

Event summary

Timeline bucket
January 05, 2017
Product types
Food
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Coca-Cola Consolidated

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

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

Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.

F-1344-2017
Recall number
F-1344-2017
Initiated
January 05, 2017
Classification
Class III
Status
Terminated
Recalling firm
Coca-Cola Consolidated
Quantity
297 cases (8 bottles/case)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).

Code information

Date Code MAR2717syf

Distribution pattern

NC