RecallHawk
Class II Recall

Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case.

Amin Trading Agency LLC

Summary

The FDA issued a Class II for Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per ca by Amin Trading Agency LLC. Reason: Product may be contaminated with Salmonella.

Details

Source

Food Recall

External ID

F-1018-2023

Action Date

2023-07-12

Status

Terminated

Category

food

Product Description

Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case.

Lot/Code Info: 20640 455AA

Quantity Affected: 24,384 sachets

Reason for Recall

Product may be contaminated with Salmonella

Distribution

Distributed to retail stores in GA, NC, OH, MD, TN, TX, MS, FL, VA, NJ, and NY.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-01

Company

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 228 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Amin Trading Agency LLC has 3 FDA actions in our database, including 3 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 (Amin Trading Agency LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Amin Trading Agency LLC have FDA actions?

Amin Trading Agency LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1018-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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