CLASS I Food recall · Reported 26 Nov 2025 · FDA Enforcement Report

Rockport Lobser Bisque recalled by Plenus Group

Plenus Group is recalling Rockport Lobser Bisque, distributed in 10 states. The recall was initiated on 29 Oct 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesa. 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 recalled130 cases (product code 4031) and 529 cases (product code 2031)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: H-0201-2026
FDA event ID: 97905
Recalling firm: Plenus Group, Lowell, MA
Brand: Rockport Lobser
Classification: Class I
Status: Terminated
Recall initiated: 29 Oct 2025
FDA classified: 19 Nov 2025
Reported: 26 Nov 2025
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Undeclared Fish & Shellfish
Product category: Soup

Timeline

29 Oct 2025	Recall initiated by company
19 Nov 2025	Classified by FDA	+21 days
26 Nov 2025	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Products contain undeclared shrimp (crustacean shellfish)

Product as listed by the FDA

Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches

Where it was distributed

Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory)

Florida Illinois Massachusetts Michigan New Hampshire Pennsylvania Puerto Rico Rhode Island Tennessee Vermont

Questions about this recall

Why was it recalled?

Products contain undeclared shrimp (crustacean shellfish)

Which lots are affected?

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

Where was it sold?

Massachusetts, Michigan, New Hampshire, Vermont, Illinois, Florida, Pennsylvania, Rhode Island. Tennessee, and Puerto Rico (US Territory)

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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