RecallHawk
Class II Recall

65550 5 Days Meal Kit

E S Foods

Summary

The FDA issued a Class II for 65550 5 Days Meal Kit by E S Foods. Reason: Animal Crackers in Meal Kits may contain metal shavings (bronze).

Details

Source

Food Recall

External ID

F-0730-2023

Action Date

2023-04-19

Status

Terminated

Category

food

Product Description

65550 5 Days Meal Kit

Lot/Code Info: 65550 5 Days Meal Kit 051523 3053 MIL Use By: May 15, 2023 65550 5 Days Meal Kit 052123 3053 MIL Use By: May 21, 2023 65550 5 Days Meal Kit 060723 3053 MIL Use By: June 7, 2023 65550 5 Days Meal Kit 061723 3053 MIL Use By: June 17, 2023

Quantity Affected: 1,044,918 meal kits (total)

Reason for Recall

Animal Crackers in Meal Kits may contain metal shavings (bronze)

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-03

Company

E S Foods

Woodbury, NY

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

E S Foods has 15 FDA actions in our database, including 15 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 (E S Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does E S Foods have FDA actions?

E S Foods has 15 FDA actions in our database, including 15 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0730-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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