Sea Port brand, Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo size 16-20. Product of Indonesia. Distributed
Summary
The FDA issued a Class II for Sea Port brand, Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo size by Sea Port Products Corp. Reason: Shrimp may be contaminated with Cesium-137 (Cs-137)..
Details
Source
Food Recall
External ID
H-0036-2026
Action Date
2025-10-22
Status
Terminated
Category
food
Product Description
Sea Port brand, Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo size 16-20. Product of Indonesia. Distributed by Sea Port Products Corporation, Kirkland, WA. Master Case: 10/2 lbs. bags. Net weight 20lbs. UPC 10659878008617 IQF Inner Bag 2lbs: UPC 6 59878 00861 0 Sea Port brand, Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo size 16-20. Product of Indonesia. Distributed by Sea Port Products Corporation, Kirkland, WA. Master Case: 20/1 lbs. bags. Net weight 20 lbs. UPC 10659878010016 IQF Inner Bag 1lbs: UPC 6 59878 01001 9
Lot/Code Info: Master Case: 10/2 lbs. bags. Lot Code: S0502 080 C10524 IQF Inner Bag 2lbs. Lot Code: Best by May 07 2028 C10524 SO502 080 IQF Inner Bag 2lbs. Lot Code: Best by May 08 2028 C10524 SO502 080 Master Case: 20/1 lbs. bags. Lot Code: S0502 080 C10524 IQF Inner Bag 1lbs. Lot Code: Best by May 08 2028 C10524 SO502 080
Quantity Affected: 1,260 cases (10/2lbs. packs per case) and 540 cases (20/1lbs. packs per case)
Reason for Recall
Shrimp may be contaminated with Cesium-137 (Cs-137).
Distribution
Distributed in CA, HI, MT, OR, WA and American Samoa.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-22
Company
Kirkland, 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 75 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 (Sea Port Products Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Sea Port Products Corp have FDA actions?
This is the only FDA action we have on record for Sea Port Products Corp in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0036-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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