Dry dates packaged under the following brands
Reason Product contains undeclared sulfites.
Bulk Dry Apricot in clear plastic bags inside brown cardboard box… recall
Recalled by Peekay International, Inc. · Maspeth, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product contains 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
Bulk Dry Apricot in clear plastic bags inside brown cardboard box and Swan brand Dry Appricot & Keshav brand Dry Apricot in 7oz and 14oz clear plastic bags. Imported & Distributed By: Peekay International Inc. 56-12 56th Street, Maspeth, New York - 11378. U.S.A. Keshav 7oz UPC: 4386423302 Keshav 14oz UPC: 4386423303 Swan 7oz UPC: 4386413302 Swan 14oz UPC: 4386413303
Quantity: 7oz - 16 cases; 320 bags; 14oz - 8 cases; 160 bags; bulk - 44.37lbs
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.
UPC: 4386423302; UPC: 4386423303; UPC: 4386413302; UPC:4386413303
Where it was sold
Massachusetts Maryland North Carolina New York Pennsylvania Virginia
FDA's distribution note: Product distributed in MA, MD, NC, NY, PA, VA
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
- Peekay International, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 15, 2019
- In FDA report of
- Nov 6, 2019
- Terminated
- Mar 11, 2020
- FDA recall number
- F-0128-2020 · event 84053
- Official record
- FDA enforcement report search