CLASS II Food recall · Reported 23 Aug 2017 · FDA Enforcement Report

HLSC Summer Herb Crusted Cod recalled by High Liner Foods

High Liner Foods is recalling HLSC Summer Herb Crusted Cod, distributed nationwide in the US. The recall was initiated on 9 Jun 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Number: 0027056190; 0027056290; 0027114190; 0027115290
Quantity recalled693,408 cases (total for all products)

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
F-2632-2017
FDA event ID
77489
Recalling firm
High Liner Foods, Portsmouth, NH
Classification
Class II
Status
Terminated
Recall initiated
9 Jun 2017
FDA classified
15 Aug 2017
Reported
23 Aug 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Fish

Timeline

9 Jun 2017Recall initiated by company
15 Aug 2017Classified by FDA+67 days
23 Aug 2017Published in enforcement report+8 days

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

Reason for recall

Product may contain undeclared milk.

Product as listed by the FDA

HLSC 12/10oz Summer Herb Crusted Cod Item Number: 1029449

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is HLSC Summer Herb Crusted Cod recalled?

Yes. High Liner Foods recalled HLSC Summer Herb Crusted Cod on 9 Jun 2017. The recall is Class II and its status is Terminated. Recall number F-2632-2017.

Why was it recalled?

Product may contain undeclared milk.

Which lots are affected?

Lot Number: 0027056190; 0027056290; 0027114190; 0027115290

Where was it sold?

Nationwide

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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