MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy peel shell on 26/30 count per pound. Net 16oz. Product is packa
Summary
The FDA issued a Class II for MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy peel shell on 26/30 cou by DIRECT SOURCE SEAFOOD LLC. Reason: Shrimp may be contaminated with Cesium-137 (Cs-137)..
Details
Source
Food Recall
External ID
H-0380-2026
Action Date
2026-01-14
Status
Terminated
Category
food
Product Description
MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy peel shell on 26/30 count per pound. Net 16oz. Product is packaged in a clear flexible plastic package with brown label and blue and green printing. UPC is 0 41735 01358 3. Product of Indonesia. PROUDLY DISTRIBUTED BY PRICE CHOPPER, INC. SCHENECTADY, NY 12306.
Lot/Code Info: DSBMS2557 25112 Best By: 04/22/27 DS503 139 T DSBMS2557 25113 Best By: 04/23/27 DS503 139 T DSBMS2557 25114 Best By: 04/24/27 DS503 080 T DSBMS2558 25116 Best By: 04/26/27 DS504 080 T DSBMS2558 25117 Best By: 04/27/27 DS504 139 T Code is interpreted as follows: DS = Direct Source Seafood BMS = Bahari Makmur Sejati 2557 = code assigned to imported container 2558 = code assigned to imported container 25113, 25114, 25116, 25117 = Julian date of production DS503 or DS504 = Plant-specific code
Quantity Affected: MARKET 32 = 3290 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
Bellevue, 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 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-0380-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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