CLASS II Food recall · Reported 21 Sep 2016 · FDA Enforcement Report

Tortilla Encrusted Breader for Tilapia recalled

Southeastern Mills Custom Seasoning Solutions is recalling Tortilla Encrusted Breader for Tilapia, distributed in Virginia. The recall was initiated on 7 Jul 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesItem #100032591, Lot # 1061674
Quantity recalled87/40 lb. Bags (3480 Pounds)

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-2283-2016
FDA event ID
74646
Classification
Class II
Status
Terminated
Recall initiated
7 Jul 2016
FDA classified
15 Sep 2016
Reported
21 Sep 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
E. coli
Product category
Bread

Timeline

7 Jul 2016Recall initiated by company
15 Sep 2016Classified by FDA+70 days
21 Sep 2016Published in enforcement report+6 days

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

Reason for recall

Product was manufactured with flour recalled by General Mills due to Ecoli contaminated.

Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.

Product as listed by the FDA

Tortilla Encrusted Breader for Tilapia, Net Wt. 40 lbs, Sm# 1000323591, MFG For High Liner Foods, Newport News, VA 23603.

Where it was distributed

VA

Virginia

Questions about this recall

Why was it recalled?

Product was manufactured with flour recalled by General Mills due to Ecoli contaminated.

Which lots are affected?

Item #100032591, Lot # 1061674

Where was it sold?

VA

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 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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