Smilin' Bob's Key West Original Smoked Fish Dip 8oz plastic container with tamper proof lid 12 containers per case
Summary
The FDA issued a Class I for Smilin' Bob's Key West Original Smoked Fish Dip 8oz plastic container with tamp by Lakeview Farms, LLC.. Reason: Undeclared Allergen - Egg.
Details
Source
Food Recall
External ID
F-0093-2022
Action Date
2021-11-10
Status
Terminated
Category
food
Product Description
Smilin' Bob's Key West Original Smoked Fish Dip 8oz plastic container with tamper proof lid 12 containers per case
Lot/Code Info: UPC 5857500400 Best By 12/19/21 Product Number 007921
Quantity Affected: 5532 containers (461 cases)
Reason for Recall
Undeclared Allergen - Egg
Distribution
Product was distributed to the following states: GA and FL
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-20
Company
Delphos, OH
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 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lakeview Farms, LLC. has 4 FDA actions in our database, including 4 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 (Lakeview Farms, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lakeview Farms, LLC. have FDA actions?
Lakeview Farms, LLC. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0093-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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