Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6
Summary
The FDA issued a Class II for Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. by AZ Gems, Inc.. Reason: elevated levels of chloramphenicol in frozen shrimp.
Details
Source
Food Recall
External ID
H-0401-2026
Action Date
2026-01-21
Status
Ongoing
Category
food
Product Description
Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6
Lot/Code Info: Product Codes: 231874 4D20 & 231874 4D21 Best By: 4/19/2026 & 4/20/2026
Quantity Affected: 1099 cases
Reason for Recall
elevated levels of chloramphenicol in frozen shrimp
Distribution
Product was shipped nationwide and distributed exclusively under the Member's Mark label.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-04
Company
Redlands, 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 54 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 (AZ Gems, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does AZ Gems, Inc. have FDA actions?
This is the only FDA action we have on record for AZ Gems, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0401-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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