Lobster Bisque Recall: Plenus Group packaging 2x8lb 4x4lb
Announced 2025-11-26 · FDA
FDA is recalling Plenus Group Inc.'s Rockport Lobser Bisque due to undeclared shrimp. The recall covers 130 cases (product code 4031) and 529 cases (product code 2031) distributed across MA, MI, NH, VT, IL, FL, PA, RI, TN and Puerto Rico, with multiple lot numbers and production dates involved. Corrective action information is not provided.
| Brand | Plenus Group Inc. |
|---|---|
| Product | Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches |
| Reason | Products contain undeclared shrimp (crustacean shellfish) |
| Severity | critical |
| Units affected | 130 |
| Distribution | Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory) |
| Agency | FDA |
| Recall / campaign no. | 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 |
WHAT YOU SHOULD DO
- Check your freezer or pantry for the recalled Rockport Lobser Bisque and do not use it if found.
- If affected, discard the product or return it to the place of purchase for a refund.
- Watch for any symptoms of shellfish allergy if exposure occurred and seek medical advice if needed.
- For questions, contact the FDA or Plenus Group for instructions.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.