Kroger Raw Colossal EZ Peel Shrimp, net wt. 2lbs., UPC 20011110643906. Product is packaged in transparent printed bag wi
Summary
The FDA issued a Class II for Kroger Raw Colossal EZ Peel Shrimp, net wt. 2lbs., UPC 20011110643906. Product i by Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.. Reason: Shrimp may be contaminated with Cesium-137 (Cs-137)..
Details
Source
Food Recall
External ID
H-0157-2026
Action Date
2025-11-12
Status
Ongoing
Category
food
Product Description
Kroger Raw Colossal EZ Peel Shrimp, net wt. 2lbs., UPC 20011110643906. Product is packaged in transparent printed bag with a blue band on the top with yellow and red details.
Lot/Code Info: lot code 10662 5085 10, Best If Used By: 03 26 27 lot code 10662 5097 11, Best If Used By: 04 07 27 lot code 10662 5106 11, Best If Used By: 04 16 27 lot code 10662 5107 10, Best If Used By: 04 17 27 lot code 10662 5111 11, Best If Used By: 04 21 27 lot code 10662 5112 10, Best If Used By: 04 22 27 lot code 10662 5113 10, Best If Used By: 04 23 27 lot code 10662 5113 11, Best If Used By: 04 23 27 lot code 10662 5114 10, Best If Used By: 04 24 27 lot code 10662 5114 11, Best If Used By: 04 24 27 Lot code 10662 5123 10, Best If Used By: 05 03 27 lot code 10062 5124 11, Best If Used By: 05 04 27
Quantity Affected: 5400 cases (3/2lbs. Pkgs per case)
Reason for Recall
Shrimp may be contaminated with Cesium-137 (Cs-137).
Distribution
Nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-20
Company
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 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. has 12 FDA actions in our database, including 12 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 (Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. have FDA actions?
Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0157-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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