CLASS I Food recall · Reported 1 Apr 2015 · FDA Enforcement Report
Vital Wheat Gluten Agridient paper sack recalled
Agridient is recalling Vital Wheat Gluten Agridient paper sack, distributed nationwide in the US. The recall was initiated on 5 Feb 2015 and the FDA has classified it as Class I.
Check your package
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-1618-2015
- FDA event ID
- 70595
- Recalling firm
- Agridient, Farmington Hills, MI
- Brand
- Vital
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 5 Feb 2015
- FDA classified
- 26 Mar 2015
- Reported
- 1 Apr 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Peanuts
- Product category
- Other
Timeline
| 5 Feb 2015 | Recall initiated by company | |
| 26 Mar 2015 | Classified by FDA | +49 days |
| 1 Apr 2015 | Published 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
Agridient Inc. received information that gluten they had repackaged and distributed contained undeclared allergen peanut. Agridient Inc. distributed gluten with undeclared allergen peanut to two customers and issued notice of recall to one customer on 02/05/2015, and the second customer on 02/21/2015 via emailed letter.
Product as listed by the FDA
Vital Wheat Gluten Agridient, 50 lb. paper sack
Where it was distributed
Domestic: Two customers- National City/Twin City 130 Hardman Ave S South St. Paul, MN 55075 EPI Breads 4710 W Ledbetter Dr. Dallas, TX 75236 Foreign: None
Questions about this recall
Why was it recalled?
Agridient Inc. received information that gluten they had repackaged and distributed contained undeclared allergen peanut. Agridient Inc. distributed gluten with undeclared allergen peanut to two customers and issued notice of recall to one customer on 02/05/2015, and the second customer on 02/21/2015 via emailed letter.
Which lots are affected?
Production date: December 2014 Expiry date: December 2017 Batch No. NO81114-P3 Lot 53656 & Batch No. N081114-P3, Lot 53657 net wt 50#
Where was it sold?
Domestic: Two customers- National City/Twin City 130 Hardman Ave S South St. Paul, MN 55075 EPI Breads 4710 W Ledbetter Dr. Dallas, TX 75236 Foreign: None
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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