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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80278

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

Open FDA event record

Event summary

Timeline bucket
June 08, 2018
Product types
Food
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Golden Star Wholesale 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

Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case

F-1597-2018
Recall number
F-1597-2018
Initiated
June 08, 2018
Classification
Class I
Status
Terminated
Recalling firm
Golden Star Wholesale Inc
Quantity
816 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Golden Star Wholesale, Inc. initiated a voluntary recall of Al Reef dried apricot sour, 12 oz., due to undeclared sulfites.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Golden Star Wholesale, Inc. initiated a voluntary recall of Al Reef dried apricot sour, 12 oz., due to undeclared sulfites.

Code information

Product Code: 061 Dates of distribution: 11/09/2017-05/29/2018

Distribution pattern

Domestic: MI, NY,MN,KY,WI,FL,NC,VA,OR,MA,OH,TX,MO Foreign:None