Seasoned Pollack Roe distributed in un-labeled plastic containers 6oz and 8oz. Containers were then labeled at H-mart,
Summary
The FDA issued a Class II for Seasoned Pollack Roe distributed in un-labeled plastic containers 6oz and 8oz. by Lemonland Food Corp. Reason: Seasoned Pollack Roe was recalled due to undeclared fish (Pollock) and R40..
Details
Source
Food Recall
External ID
F-0655-2023
Action Date
2023-04-05
Status
Terminated
Category
food
Product Description
Seasoned Pollack Roe distributed in un-labeled plastic containers 6oz and 8oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
Lot/Code Info: Feb. 16, 2023 to Feb. 23, 2023.
Quantity Affected: 6oz containers = 6.48 lb; 8oz containers = 15.4 lb.
Reason for Recall
Seasoned Pollack Roe was recalled due to undeclared fish (Pollock) and R40.
Distribution
Distributed in Washington
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-23
Company
Kent, WA
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.
Lemonland Food Corp has 44 FDA actions in our database, including 44 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 (Lemonland Food Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lemonland Food Corp have FDA actions?
Lemonland Food Corp has 44 FDA actions in our database, including 44 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0655-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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