Al Reef dried apricot sour recall
Recalled by Golden Star Wholesale Inc · Troy, MI, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Golden Star Wholesale, Inc. initiated a voluntary recall of Al Reef dried apricot sour, 12 oz., due to undeclared sulfites.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
Quantity: 816 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Product Code: 061 Dates of distribution: 11/09/2017-05/29/2018
Where it was sold
Florida Kentucky Massachusetts Michigan Minnesota Missouri North Carolina New York Ohio Oregon Texas Virginia Wisconsin
FDA's distribution note: Domestic: MI, NY,MN,KY,WI,FL,NC,VA,OR,MA,OH,TX,MO Foreign:None
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Golden Star Wholesale Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 8, 2018
- In FDA report of
- Jul 4, 2018
- Terminated
- Oct 16, 2018
- FDA recall number
- F-1597-2018 · event 80278
- Official record
- FDA enforcement report search