FDA Recall United States Terminated 2026 recordClass II
DIRECT SOURCE SEAFOOD LLC
- Product
- MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy pee…
- Published
- January 14, 2026
- Distribution
- Market 32 brand frozen raw shrimp was so…
DIRECT SOURCE SEAFOOD LLC Recall: Shrimp may be contaminated with Cesium-137 (Cs-137).
United States
TerminatedClass II
- Company
- DIRECT SOURCE SEAFOOD LLC
- Product
- waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TA…
- Recall date
- December 18, 2025
- Terminated
- April 7, 2026
- Source
- FDA
Reason for recall
Shrimp may be contaminated with Cesium-137 (Cs-137).
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | Not published in this source record | waterfront Bistro shrimp = 1800 cases | 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 |
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.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0379-2026
- Event ID
- 98182
- Status
- Terminated
- Classification
- Class II
- Company
- DIRECT SOURCE SEAFOOD LLC
- 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.
- Quantity
- waterfront Bistro shrimp = 1800 cases
- Reason
- Shrimp may be contaminated with Cesium-137 (Cs-137).
- Recall initiation date
- December 18, 2025
- Report date
- January 14, 2026
- Classification date
- Not published in this source record
- Termination date
- April 7, 2026
- Distribution pattern
- 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.
- UPC, lot, and code information
- 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 98182 with 1 other product entry in Public Health Trace.
Responsible company: DIRECT SOURCE SEAFOOD LLC
Other recalls from DIRECT SOURCE SEAFOOD LLC
FDA Recall United States Terminated 2026 recordClass II
DIRECT SOURCE SEAFOOD LLC
- Product
- MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy pee…
- Published
- January 14, 2026
- Distribution
- Market 32 brand frozen raw shrimp was so…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Connecticut | 1 |
| Massachusetts | 1 |
| New Hampshire | 1 |
| New York | 1 |
| Pennsylvania | 1 |
| Vermont | 1 |
| Colorado | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Montana | 1 |
| North Dakota | 1 |
| Nevada | 1 |
| Oregon | 1 |
| Utah | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
