Mary s Gone Crackers Super Seed Seaweed & Black Sesame Crackers Product Item number: 10033380101 UPC: 8 53665 00510 7
Summary
The FDA issued a Class II for Mary s Gone Crackers Super Seed Seaweed & Black Sesame Crackers Product Item n by Mary's Gone Crackers. Reason: Product may be contaminated with foreign material.
Details
Source
Food Recall
External ID
F-0689-2023
Action Date
2023-04-05
Status
Terminated
Category
food
Product Description
Mary s Gone Crackers Super Seed Seaweed & Black Sesame Crackers Product Item number: 10033380101 UPC: 8 53665 00510 7
Lot/Code Info: Lot codes: 4CKR5734 - Expiration: 03/02/2024 4CKR5735 - Expiration: 03/02/2024 4CKR5736 - Expiration: 03/02/2024 4CKR5737 - Expiration: 03/03/2024 4CKR5738 - Expiration: 03/03/2024
Quantity Affected: 2,376 6pk cases
Reason for Recall
Product may be contaminated with foreign material
Distribution
Throughout the USA.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-15
Company
Reno, NV
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 66 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-0689-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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