Plenus Group Inc. Recall: Products contain undeclared shrimp (crustacean shellfish)
United States
TerminatedClass I
- Company
- Plenus Group Inc.
- Product
- Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b…
- Recall date
- October 29, 2025
- Terminated
- February 25, 2026
- Source
- FDA
Reason for recall
Products contain undeclared shrimp (crustacean shellfish)
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches | Not published in this source record | 130 cases (product code 4031) and 529 cases (product code 2031) | 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 |
Distribution
- Massachusetts
- Michigan
- New Hampshire
- Vermont
- Illinois
- Florida
- Pennsylvania
- Rhode Island. Tennessee
- and Puerto Rico (US Territory)
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0201-2026
- Event ID
- 97905
- Status
- Terminated
- Classification
- Class I
- Company
- Plenus Group Inc.
- Product description
- Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches
- Quantity
- 130 cases (product code 4031) and 529 cases (product code 2031)
- Reason
- Products contain undeclared shrimp (crustacean shellfish)
- Recall initiation date
- October 29, 2025
- Report date
- November 26, 2025
- Classification date
- Not published in this source record
- Termination date
- February 25, 2026
- Distribution pattern
- Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory)
- UPC, lot, and code information
- 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Plenus Group Inc.
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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
