CLASS III Food recall · Reported 15 Aug 2012 · FDA Enforcement Report

Dried Brewers Yeast TG_YFS004 Naturex 375 Huyler Street recalled

Naturex is recalling Dried Brewers Yeast TG_YFS004 Naturex 375 Huyler Street, South Hackensack, NJ 07606 USA, distributed in New Jersey, South Carolina. The recall was initiated on 18 Apr 2012 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot #0215/007/A11 Lot #C308/029/A11
Quantity recalled4500 kg

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-1858-2012
FDA event ID
62653
Recalling firm
Naturex, S Hackensack, NJ
Classification
Class III
Status
Terminated
Recall initiated
18 Apr 2012
FDA classified
7 Aug 2012
Reported
15 Aug 2012
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons
Product category
Other

Timeline

18 Apr 2012Recall initiated by company
7 Aug 2012Classified by FDA+111 days
15 Aug 2012Published 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

The affected lots were tested and found to contain an unusual high level of selenium.

Product as listed by the FDA

Dried Brewers Yeast TG_YFS004 Naturex 375 Huyler Street, South Hackensack, NJ 07606 USA Phone: 1 201 440 5000 Net Wt 25 kg

Where it was distributed

1 firm in New Jersey and 1 firm in South Carolina

New JerseySouth Carolina

Questions about this recall

Why was it recalled?

The affected lots were tested and found to contain an unusual high level of selenium.

Which lots are affected?

Lot #0215/007/A11 Lot #C308/029/A11

Where was it sold?

1 firm in New Jersey and 1 firm in South Carolina

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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