Recall record at a glance
| Official record | F-0128-2020 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Peekay International, Inc. |
| Report date | Nov 6, 2019 |
| Recall initiation date | Oct 15, 2019 |
| Quantity | 7oz - 16 cases; 320 bags; 14oz - 8 cases; 160 bags; bulk - 44.37lbs |
| Location | Maspeth, NY, United States |
Official product description
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
Why the product was recalled
Product contains undeclared sulfites
Distribution information
Product distributed in MA, MD, NC, NY, PA, VA
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.