FDA recall record
Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of October 16, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
Reason
Golden Star Wholesale, Inc. initiated a voluntary recall of Al Reef dried apricot sour, 12 oz., due to undeclared sulfites.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
Code information listed by FDA
Product Code: 061 Dates of distribution: 11/09/2017-05/29/2018
Distribution and firm information
Recalling firm listed by FDA: Golden Star Wholesale Inc
Firm location listed by FDA: Troy, MI, United States
Distribution reported by FDA: Domestic: MI, NY,MN,KY,WI,FL,NC,VA,OR,MA,OH,TX,MO Foreign:None
Product quantity listed by FDA: 816 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.