RecallHawk
Class II Recall

Tops GOLD Khatta Meetha Pickle NET QTY.: 33.51oz PRODUCT OF INDIA UPC: 8904288611427 INGREDIENTS:***Mustard Oil***

Mangalm LLC

Summary

The FDA issued a Class II for Tops GOLD Khatta Meetha Pickle NET QTY.: 33.51oz PRODUCT OF INDIA UPC: 890428861 by Mangalm LLC. Reason: Potential adulteration with erucic acid from mustard oil ingredient..

Details

Source

Food Recall

External ID

H-0627-2026

Action Date

2026-04-01

Status

Ongoing

Category

food

Product Description

Tops GOLD Khatta Meetha Pickle NET QTY.: 33.51oz PRODUCT OF INDIA UPC: 8904288611427 INGREDIENTS:***Mustard Oil***

Lot/Code Info: UPC: 8904288611427

Quantity Affected: 40 cases (12 - 33.51 oz. cans/case)

Reason for Recall

Potential adulteration with erucic acid from mustard oil ingredient.

Distribution

U.S. Distribution: CA, NV, OR, UT, WA. Foreign Distribution: None.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-01-24

Company

Mangalm LLC

Newark, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Mangalm LLC has 8 FDA actions in our database, including 8 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mangalm LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mangalm LLC have FDA actions?

Mangalm LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0627-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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