RecallHawk
Class II Recall

Super Seed Everything Crackers 5.5 oz. UPC: 8 53665 00509 1

Mary's Gone Crackers

Summary

The FDA issued a Class II for Super Seed Everything Crackers 5.5 oz. UPC: 8 53665 00509 1 by Mary's Gone Crackers. Reason: May contain foreign object: rubber pieces.

Details

Source

Food Recall

External ID

F-0223-2023

Action Date

2023-01-11

Status

Terminated

Category

food

Product Description

Super Seed Everything Crackers 5.5 oz. UPC: 8 53665 00509 1

Lot/Code Info: Lot number: 4CKR5410, Expiration date: 12/09/2023

Quantity Affected: 1,076 cases

Reason for Recall

May contain foreign object: rubber pieces

Distribution

Product was distributed to 8 distributors located in CA, IA, MD, NJ, GA, and WI.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-12-20

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

Mary's Gone Crackers 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 (Mary's Gone Crackers) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mary's Gone Crackers have FDA actions?

Mary's Gone Crackers 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-0223-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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