VerifyRecall
Alerts
RECALL RECORD — CLASS IRecall closedF-0205-2017/FDA enforcement
Qualitech, INC·Food·Jul 5, 2016

Fe Rainbow Blend, Product Code 22795

What you need to know

Class I

  • What happened

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

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Some E. coli strains produce toxins that can cause severe, sometimes bloody diarrhea.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDAAZ, CA, GA, ID +6 moreMore food

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Share via WhatsApp

Match before you discard

Product identification

Source: FDA FOOD

Brand nameQualitech, INC
Recalling firmQualitech, INCChaska, MN, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot: 31950
Distribution area
AZCAGAIDILINMIMNTXWA

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

United States, Canada

Quantity affected1, 400 lbs.
Recall initiationFDA report date: October 26, 2016
FDA recall numberF-0205-2017

Beyond the headline

The recall, in context

Qualitech, INC initiated this food recall on July 5, 2016. The FDA enforcement report states: QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria. The FDA report lists distribution as: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

The FDA enforcement report describes the reason as: QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

Fe Rainbow Blend, Product Code 22795 was made or distributed by Qualitech, INC in Chaska, MN, United States. This page reflects FDA report F-0205-2017, dated October 26, 2016.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, some E. coli strains produce toxins that can cause severe, sometimes bloody diarrhea.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

E. coli

Symptoms to watch for

Severe stomach cramps, diarrhea, vomiting and sometimes a low fever. Bloody diarrhea or signs of dehydration need prompt medical attention.

When symptoms may appear

Usually 3 to 4 days after exposure, with a range of roughly 1 to 10 days.

Higher-risk groups

Young children, older adults, pregnant people and people with weakened immune systems are at higher risk of complications.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Fe Rainbow Blend, Product Code 22795 recall?

Qualitech, INC recalled Fe Rainbow Blend, Product Code 22795 in an FDA Class I enforcement action reported as F-0205-2017. QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

What are the symptoms of E. coli exposure?

Severe stomach cramps, diarrhea, vomiting and sometimes a low fever. Bloody diarrhea or signs of dehydration need prompt medical attention.

How quickly can E. coli symptoms appear?

Usually 3 to 4 days after exposure, with a range of roughly 1 to 10 days.

Who is most at risk from E. coli?

Young children, older adults, pregnant people and people with weakened immune systems are at higher risk of complications.

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

How do I get a refund from Qualitech, INC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0205-2017 and keep the packaging, lot code and proof of purchase if you have them.

Is the Qualitech, INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0205-2017. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Qualitech, INC

View brand
Class I·

Qualitech, INC

Fe Bacon 286, Product Code 22286

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

AZ, CA, GA +7 more +1 countriesFood
Class I·

Qualitech, INC

Fe Red Bell Pepper, Product Code 22708

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

AZ, CA, GA +7 more +1 countriesFood

Related alerts

Recent E. coli recalls

All alerts
Class II·

Prosperity Organic Foods INC

Miyoko's Creamery European Style Salted Plant Milk Butter, NET WT

Product recalled due to yeast, mold, and E. coli.

IN, CT, FL +7 moreFood
Class I·

Berlin Seeds

Alfalfa Sprouting Seeds, Packaged in 1/4 lb., 1/2 lb., 1 lb., and 5 lb

Product contains alfalfa seed recalled by the supplier due to potential E. coli and/or Salmonella contamination.

Nationwide (US)Food

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.