Class IFood recall: undeclared shellfish
Rockport Lobser Bisque
Plenus Group Inc., of Lowell, MA, began recalling this product on . FDA classified the recall as Class I on .
Why it was recalled
In FDA’s words:
Products contain undeclared shrimp (crustacean shellfish)
The allergen tags on this page are ours, matched from FDA’s words above.
The product
Rockport Lobser Bisque
Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches
- Codes and dates
- 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
- 130 cases (product code 4031) and 529 cases (product code 2031)
- Recall number
- H-0201-2026
Where it was distributed
In FDA’s words:
Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory)
What Class I means
In FDA’s definitions, a Class I recall is one where: there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. FDA’s recall definitions
If you have this product
- FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
- FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
- If someone has a serious allergic reaction, call 911. Signs of a serious reaction
Source
FDA’s Enforcement Report, read through openFDA. This recall first appeared in the report of . openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.