CLASS I Food recall · Reported 27 Nov 2019 · FDA Enforcement Report

Dry dates packaged under the following brands recalled

Peekay International is recalling Dry dates packaged under the following brands: Keshav Dry Yellow Dates, distributed in 10 states. The recall was initiated on 5 Nov 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest Before: 2-12-22
Quantity recalled55 Lbs.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0197-2020
FDA event ID
84225
Recalling firm
Peekay International, Maspeth, NY
Brand
Dry
Classification
Class I
Status
Terminated
Recall initiated
5 Nov 2019
FDA classified
26 Nov 2019
Reported
27 Nov 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sulfites
Product category
Other

Timeline

5 Nov 2019Recall initiated by company
26 Nov 2019Classified by FDA+21 days
27 Nov 2019Published in enforcement report+1 day

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains undeclared sulfites.

Product as listed by the FDA

Dry dates packaged under the following brands: Keshav Dry Yellow Dates, 7oz., UPC: 643864233124 and 14oz., UPC: 643864233131; and Swan Dry Yellow Dates, 7 oz., UPC: 643864136623 and 14oz., UPC: 643864136630. Product is in a clear plastic pouch (or explain the packaging).

Where it was distributed

CT, FL, MA, MD, NC, NH, NY, OH, PA, & VA

ConnecticutFloridaMassachusettsMarylandNorth CarolinaNew HampshireNew YorkOhioPennsylvaniaVirginia

Questions about this recall

Is Dry dates packaged under the following brands: Keshav Dry Yellow Dates recalled?

Yes. Peekay International recalled Dry dates packaged under the following brands: Keshav Dry Yellow Dates on 5 Nov 2019. The recall is Class I and its status is Terminated. Recall number F-0197-2020.

Why was it recalled?

Product contains undeclared sulfites.

Which lots are affected?

Best Before: 2-12-22

Where was it sold?

CT, FL, MA, MD, NC, NH, NY, OH, PA, & VA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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