RecallHawk
Class II Recall

waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count per Lb. Net wt. 32oz (2LB). Produc

DIRECT SOURCE SEAFOOD LLC

Summary

The FDA issued a Class II for waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 by DIRECT SOURCE SEAFOOD LLC. Reason: Shrimp may be contaminated with Cesium-137 (Cs-137)..

Details

Source

Food Recall

External ID

H-0379-2026

Action Date

2026-01-14

Status

Terminated

Category

food

Product Description

waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count per Lb. Net wt. 32oz (2LB). Product is packaged in white flexible plastic pouch with multicolored labeling. UPC is 0 21130 13224 9. Product of Indonesia. DISTRIBUTED BY LUCERNE FOODS, INC. P.O. BOX 99 PLEASANTON, CA 94566.

Lot/Code Info: DSBMS2559 25115 S5060-5100 Best If Used By: APR 25 2027 DSBMS2559 25116 S5060-5100 Best If Used By: APR 26 2027 Code is interpreted as follows: DS = Direct Source Seafood BMS = Bahari Makmur Sejati 2559 = code assigned to imported container 25115 = Julian date of production 25116 = Julian date of production S5060-5100 = Plant-specific code

Quantity Affected: waterfront Bistro shrimp = 1800 cases

Reason for Recall

Shrimp may be contaminated with Cesium-137 (Cs-137).

Distribution

Market 32 brand frozen raw shrimp was sold in CT, MA, NH, NY, PA, and VT. waterfront BISTRO frozen raw shrimp was sold in CO, IA, ID, IL, IN, MT, ND, NV, OR, UT, and WY.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-18

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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.

DIRECT SOURCE SEAFOOD LLC has 2 FDA actions in our database, including 2 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 (DIRECT SOURCE SEAFOOD LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does DIRECT SOURCE SEAFOOD LLC have FDA actions?

DIRECT SOURCE SEAFOOD LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0379-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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