CLASS II Food recall · Reported 25 May 2016 · FDA Enforcement Report

Commercial Wheat Germ recalled by UNFI

Unfi is recalling Commercial Wheat Germ 274000, distributed in 16 states. The recall was initiated on 15 Apr 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Codes: W121915, W012116, W122315
Quantity recalled32 bags

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-1363-2016
FDA event ID
73934
Recalling firm
Unfi, Chesterfield, NH
Classification
Class II
Status
Terminated
Recall initiated
15 Apr 2016
FDA classified
17 May 2016
Reported
25 May 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
E. coli
Product category
Fish

Timeline

15 Apr 2016Recall initiated by company
17 May 2016Classified by FDA+32 days
25 May 2016Published 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 contains generic E. coli.

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

COMMERCIAL WHEAT GERM 274000, 50.00 lbs. (22.68 kg); UPC Code: 0-26938-46535-3

Where it was distributed

NY, RI, ME, MA, VT, OH, MN, IN, KY, MO, ME, SD, CT, IA, NE, WI, NJ

ConnecticutIowaIndianaKentuckyMassachusettsMaineMinnesotaMissouriNebraskaNew JerseyNew YorkOhioRhode IslandSouth DakotaVermontWisconsin

Questions about this recall

Why was it recalled?

Product contains generic E. coli.

Which lots are affected?

Lot Codes: W121915, W012116, W122315

Where was it sold?

NY, RI, ME, MA, VT, OH, MN, IN, KY, MO, ME, SD, CT, IA, NE, WI, NJ

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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