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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71870

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

Open FDA event record

Event summary

Timeline bucket
August 04, 2015
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Dr. Pepper Snapple Group 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

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

A&W Cream Soda 12 FL OZ (355 mL)

F-3079-2015
Recall number
F-3079-2015
Initiated
August 04, 2015
Classification
Class II
Status
Terminated
Quantity
10,292 cases (12 cans/case)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The American Bottling Company is recalling 12 oz. cans of A& W Cream Soda because the front panel bears the statement "caffeine free" and the product contains caffeine

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The American Bottling Company is recalling 12 oz. cans of A& W Cream Soda because the front panel bears the statement "caffeine free" and the product contains caffeine

Code information

Lot Codes: G5184VE and G5195VE

Distribution pattern

U.S. distribution to the following; CA, NV, and ID. No foreign consignees.