Summary
The FDA issued a Class I for Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches by Plenus Group Inc.. Reason: Products contain undeclared shrimp (crustacean shellfish).
Details
Source
Food Recall
External ID
H-0201-2026
Action Date
2025-11-26
Status
Terminated
Category
food
Product Description
Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches
Lot/Code Info: a. 2x8lb pouch with Production Date: 09/05/2025, MFG Code: 25248, Best By Date: 03/06/2027, Lot Number: 069161 b. 2x8lb pouch with Production Date: 09/05/2025, MFG Code: 25248, Best By Date: 03/06/2027, Lot Number: 069162 c. 2x8lb pouch with Production Date: 09/11/2025, MFG Code: 25254, Best By Date: 03/12/2027, Lot Number: 069321 d. 2x8lb pouch with Production Date: 09/11/2025; MFG Code: 25254, Best By Date: 03/12/2025, Lot Number 069322 e. 4x4lb pouch with Production Date: 09/12/2025, MFG Code: 25255, Best By Date: 03/13/2027, Lot Number: 069323 f. 2x8lb pouch with Production Date: 09/30/2025, MFG Code: 25273, Best By Date: 03/31/2027, Lot Number: 070042 g. 2x8lb pouch with Production Date: 09/30/2025, MFG Code: 25273, Best By Date: 03/31/2027, Lot Number: 070043 h. 4x4lb pouch with Production Date: 09/30/2025, MFG Code: 25273, Best By Date: 03/31/2027, Lot Number: 070064
Quantity Affected: 130 cases (product code 4031) and 529 cases (product code 2031)
Reason for Recall
Products contain undeclared shrimp (crustacean shellfish)
Distribution
Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory)
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-29
Company
Lowell, MA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Plenus Group Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Plenus Group Inc. have FDA actions?
This is the only FDA action we have on record for Plenus Group Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0201-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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