FindMyRecallSubscribe
Class I: serious health riskTerminated

QualiTech FE Green Bell Pepper Recall

FE Green Bell Pepper, Product Code 22733

QualiTech, Inc · Chaska, MN

Risk level
Class I
Reported by FDA
Oct 26, 2016
Recall ID
F-0202-2017
Check your lot numberHow we source this data

Summary

QualiTech recalled FE Green Bell Pepper starting Jul 5, 2016. The FDA classified it as Class I (serious health risk) and published enforcement report F-0202-2017 on Oct 26, 2016. Reason: QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria. Status: Terminated.

Why it was recalled

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

Product description

FE Green Bell Pepper, Product Code 22733. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA

Lot numbers, UPCs & expiration codes

Lots: 31624, 31978

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0202-2017
Classification
Class I
Status
Terminated
Recall initiated
Jul 5, 2016
FDA report date
Oct 26, 2016
Quantity
1.500 lbs.
Recall type
Voluntary: Firm initiated
Recalling firm
QualiTech, Inc

Original FDA data

Every field from FDA enforcement report F-0202-2017, exactly as published.

Show all FDA fields
City
Chaska
State
MN
Status
Terminated
Country
United States
Event ID
74650
Address
318 Lake Hazeltine Dr
Code information
Lots: 31624, 31978
Postal code
55318-1034
Report date
Oct 26, 2016
Product type
Food
Recall number
F-0202-2017
Classification
Class I
Recalling firm
QualiTech, Inc
Product quantity
1.500 lbs.
Termination date
Sep 13, 2017
Reason for recall
QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
Voluntary / mandated
Voluntary: Firm initiated
Product description
FE Green Bell Pepper, Product Code 22733. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
Distribution pattern
AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
Recall initiation date
Jul 5, 2016
Initial firm notification
E-Mail
Center classification date
Oct 19, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0202-2017, published Oct 26, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls