Vemondo Vegan Crabless Mini Crabcakes by Lidl 8.5 OUNCES (240g) coated paper box ten (10) packages per case. Frozen.
Summary
The FDA issued a Class I for Vemondo Vegan Crabless Mini Crabcakes by Lidl 8.5 OUNCES (240g) coated paper box by Cuisine Innovations Unlimited, LLC. Reason: Undeclared egg.
Details
Source
Food Recall
External ID
F-0015-2022
Action Date
2021-10-20
Status
Terminated
Category
food
Product Description
Vemondo Vegan Crabless Mini Crabcakes by Lidl 8.5 OUNCES (240g) coated paper box ten (10) packages per case. Frozen.
Lot/Code Info: Lot # 23021: 2/17/2023 Lot # 23121: 2/18/2023 Lot # 23821: 2/25/2023
Quantity Affected: 1800 cases
Reason for Recall
Undeclared egg
Distribution
Distributed to 3 distributors in MD, NC, and VA then further distributed to retail stores
Type: Voluntary: Firm initiated
Recall Initiated: 2021-09-24
Company
Lakewood, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Cuisine Innovations Unlimited, LLC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Cuisine Innovations Unlimited, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cuisine Innovations Unlimited, LLC have FDA actions?
Cuisine Innovations Unlimited, 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-0015-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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