Frozen Raw Easy Peel shrimp, IQF, 2-lb bag, 10 bags/case; Generic Brown cardboard box UPC: 021130123223
Summary
The FDA issued a Class II for Frozen Raw Easy Peel shrimp, IQF, 2-lb bag, 10 bags/case; Generic Brown cardboar by Tas Tematic Foods Inc. Reason: Product which was on FDA hold for high levels of Nitrofuran was inadvertently distributed..
Details
Source
Food Recall
External ID
H-0640-2025
Action Date
2025-10-08
Status
Terminated
Category
food
Product Description
Frozen Raw Easy Peel shrimp, IQF, 2-lb bag, 10 bags/case; Generic Brown cardboard box UPC: 021130123223
Lot/Code Info: Lot Code: 25 085 ID02 170035; Expiration Date: MAR 26 2027
Quantity Affected: 5 cases
Reason for Recall
Product which was on FDA hold for high levels of Nitrofuran was inadvertently distributed.
Distribution
Product was distributed to two (2) locations of the firm's consignee located in CA.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-29
Company
Tarzana, CA
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 39 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Tas Tematic Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tas Tematic Foods Inc have FDA actions?
This is the only FDA action we have on record for Tas Tematic Foods Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0640-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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