Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported November 26, 2025
Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches
Products contain undeclared shrimp (crustacean shellfish)
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Plenus Group Inc. recalled Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches - a critical-severity action.
Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches was recalled by Plenus Group Inc. in November 26, 2025. Reason: Products contain undeclared shrimp (crustacean shellfish). Check the official notice for the remedy. Verify recall #H-0201-2026 with the FDA Food before acting.
The recall
Plenus Group Inc. issued this critical-severity FDA Food recall-Products contain undeclared shrimp (crustacean shellfish).
- Critical
- severity level
- Class I
- classification
- November 26, 2025
- reported
Sourced from official FDA Food enforcement records. Verify recall #H-0201-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #H-0201-2026) was formally reported on November 26, 2025, with the manufacturer initiating the action on October 29, 2025. It is classified under Critical severity (Class I), with a current status of Terminated. Plenus Group Inc. is listed as the recalling firm, operating out of Lowell, MA. Federal records list the affected scope as 130 cases (product code 4031) and 529 cases (product code 2031).
The documented reason for this recall is: Products contain undeclared shrimp (crustacean shellfish) Distribution data in the federal record shows the product reached: Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory). Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
130 cases (product code 4031) and 529 cases (product code 2031)
Related Recalls
6
2 from same agency
Product description
Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches
Reason for recall
Products contain undeclared shrimp (crustacean shellfish)
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | H-0201-2026 |
| Date reported | November 26, 2025 |
| Date initiated | October 29, 2025 |
| Recalling firm | Plenus Group Inc. |
| Firm location | Lowell, MA |
| Affected scope | 130 cases (product code 4031) and 529 cases (product code 2031) |
| Distribution | Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory) |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (H-0201-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches. Recalled by Plenus Group Inc.. Units affected: 130 cases (product code 4031) and 529 cases (product code 2031).
Why was this product recalled? ▼
Products contain undeclared shrimp (crustacean shellfish)
Which agency issued this recall? ▼
This recall was issued by the FDA Food on November 26, 2025. Severity: Critical. Recall number: H-0201-2026.
Where was the recalled product distributed? ▼
Distribution: Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory).
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (H-0201-2026) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Conair Recalls Over One Million Cuisinart Grill Brushes Due… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported November 26, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.