CLASS I Food recall · Reported 26 Oct 2016 · FDA Enforcement Report

FE RedBell Pepper recalled by QualiTech

QualiTech is recalling FE RedBell Pepper 339, distributed in 10 states. The recall was initiated on 5 Jul 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot codes: 31476, 31802
Quantity recalled6,000 lbs.

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-0196-2017
FDA event ID
74650
Recalling firm
QualiTech, Chaska, MN
Classification
Class I
Status
Terminated
Recall initiated
5 Jul 2016
FDA classified
19 Oct 2016
Reported
26 Oct 2016
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
E. coli
Product category
Fish

Timeline

5 Jul 2016Recall initiated by company
19 Oct 2016Classified by FDA+106 days
26 Oct 2016Published in enforcement report+7 days

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

Reason for recall

QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

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

FE RedBell Pepper 339, Product Code 22339. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA

Where it was distributed

AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

ArizonaCaliforniaGeorgiaIdahoIllinoisIndianaMichiganMinnesotaTexasWashington

Questions about this recall

Why was it recalled?

QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

Which lots are affected?

Lot codes: 31476, 31802

Where was it sold?

AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

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.

Other products in this recall event

17 other products · FDA event 74650

This product is part of a recall event; the main page for the event is FE Jalapeno recalled by QualiTech.

More recalls from QualiTech

All 18
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