CLASS II Food recall · Reported 25 Apr 2018 · FDA Enforcement Report

Provim ESP Vita Wheat Gluten recalled by ADM Agri Industries

ADM Agri Industries is recalling Provim ESP Vita Wheat Gluten, distributed in Illinois, Maine, Michigan, North Carolina, Ohio. The recall was initiated on 8 Mar 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 04087-(01-25)-C, Expiration 09-Feb-19; Lot # 04287-40-C, Expiration 11-Feb-19; Lot # 04387-40-C, Expiration 13-Feb-19 & Lot # 04787-40-C, Expiration 16-Feb-19.C
Quantity recalled6,080/50 lb bags + 25/1653 kg totes

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-1099-2018
FDA event ID
79509
Recalling firm
ADM Agri Industries, Candiac
Classification
Class II
Status
Terminated
Recall initiated
8 Mar 2018
FDA classified
16 Apr 2018
Reported
25 Apr 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Fish

Timeline

8 Mar 2018Recall initiated by company
16 Apr 2018Classified by FDA+39 days
25 Apr 2018Published in enforcement report+9 days

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

Reason for recall

The firm was notified by their supplier that the flour used to manufacture the product tested positive for Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Provim ESP Vita Wheat Gluten, Product code 6303, 50 lb bag

Where it was distributed

Product was shipped to the following states: IL, ME, MI, NC & OH.

IllinoisMaineMichiganNorth CarolinaOhio

Questions about this recall

Why was it recalled?

The firm was notified by their supplier that the flour used to manufacture the product tested positive for Listeria monocytogenes.

Which lots are affected?

Lot # 04087-(01-25)-C, Expiration 09-Feb-19; Lot # 04287-40-C, Expiration 11-Feb-19; Lot # 04387-40-C, Expiration 13-Feb-19 & Lot # 04787-40-C, Expiration 16-Feb-19.C

Where was it sold?

Product was shipped to the following states: IL, ME, MI, NC & OH.

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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