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Peekay International, Inc. Recall: Product contains undeclared sulfites - F-0128-2020

United States

TerminatedClass I

Company
Peekay International, Inc.
Product
Bulk Dry Apricot in clear plastic bags inside brown cardboar…
Recall date
October 15, 2019
Terminated
March 11, 2020
Source
FDA

Reason for recall

Product contains undeclared sulfites

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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 4386423302 7oz - 16 cases; 320 bags; 14oz - 8 cases; 160 bags; bulk - 44.37lbs UPC: 4386423302; UPC: 4386423303; UPC: 4386413302; UPC:4386413303

Distribution

  • Product distributed in MA
  • MD
  • NC
  • NY
  • PA
  • VA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0128-2020
Event ID
84053
Status
Terminated
Classification
Class I
Company
Peekay International, Inc.
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
Quantity
7oz - 16 cases; 320 bags; 14oz - 8 cases; 160 bags; bulk - 44.37lbs
Reason
Product contains undeclared sulfites
Recall initiation date
October 15, 2019
Report date
November 6, 2019
Classification date
Not published in this source record
Termination date
March 11, 2020
Distribution pattern
Product distributed in MA, MD, NC, NY, PA, VA
UPC, lot, and code information
UPC 4386423302; UPC: 4386423302; UPC: 4386423303; UPC: 4386413302; UPC:4386413303
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Peekay International, Inc.

Other recalls from Peekay International, Inc.

FDA Recall United States TerminatedTerminated: March 11, 2020Historical recordClass I

Peekay International, Inc.

Product
Dry dates packaged under the following brands: Keshav Dry Ye…
Published
November 27, 2019
Distribution
CT, FL, MA, MD, NC, NH, NY, OH, PA, & VA

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Massachusetts 1
Maryland 1
North Carolina 1
New York 1
Pennsylvania 1
Virginia 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of March 11, 2020.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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