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Muktanand Foods Inc Recall: Undeclared sulfites

United States

TerminatedClass I

Company
Muktanand Foods Inc
Product
ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 1032…
Recall date
September 8, 2022
Terminated
December 2, 2022
Source
FDA

Reason for recall

Undeclared sulfites

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear plastic bag, 20 bags per wholesale case Not published in this source record 485 cases All product regardless of the presence or absence of a batch number on the product

Distribution

  • AL CO GA IA IL KS MN MO NC NE NJ OH SC WI

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1748-2022
Event ID
90844
Status
Terminated
Classification
Class I
Company
Muktanand Foods Inc
Product description
ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear plastic bag, 20 bags per wholesale case
Quantity
485 cases
Reason
Undeclared sulfites
Recall initiation date
September 8, 2022
Report date
September 28, 2022
Classification date
Not published in this source record
Termination date
December 2, 2022
Distribution pattern
AL CO GA IA IL KS MN MO NC NE NJ OH SC WI
UPC, lot, and code information
All product regardless of the presence or absence of a batch number on the product
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Muktanand Foods Inc

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
Alabama 1
Colorado 1
Georgia 1
Iowa 1
Illinois 1
Kansas 1
Minnesota 1
Missouri 1
North Carolina 1
Nebraska 1
New Jersey 1
Ohio 1
South Carolina 1
Wisconsin 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.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

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?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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.