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Stop using now Food recall · FDA · Published July 5, 2016

QualiTech Recalls FE Jalapenos Due to E. coli Risk

QualiTech, Inc. recalls FE Jalapeno 709 due to potential E. coli O121 contamination. Check lot numbers and distribution states for details.

🇺🇸 FDA recall #F-0200-2017FoodQualiTech ›
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Recalling firmQualiTech, Inc318 Lake Hazeltine Dr · Chaska, MN 55318-1034
✎ GovInfoNow plain-language explainer

What happened, in plain English

QualiTech, Inc. is recalling FE Jalapeno 709 because a supplier notified them that the material may contain E. coli O121 bacteria. The recall covers approximately 3,200 lbs of product distributed in several U.S. states and Canada. Consumers should check their products against the specific lot numbers listed. Read more at govinfonow.com/recall/23881-qualitech-recalls-fe-jalapenos-due-to-e-coli-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/23881-qualitech-recalls-fe-jalapenos-due-to-e-coli-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-0200-2017

Cite this page

“QualiTech Recalls FE Jalapenos Due to E. coli Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23881-qualitech-recalls-fe-jalapenos-due-to-e-coli-risk. Based on FDA recall #F-0200-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0200-2017%22&limit=1).

Why it’s dangerous

The product may contain E. coli O121 bacteria, which can cause serious illness if ingested. This is classified as a Class I recall, indicating the highest risk of adverse health consequences.

Who’s affected

Consumers and food service establishments who purchased FE Jalapeno 709 from QualiTech, Inc. in Arizona, California, Georgia, Idaho, Illinois, Indiana, Michigan, Minnesota, Texas, Washington, or Canada.

How to tell if you have this one

Look for FE Jalapeno 709 in 50 lb corrugated cases with polyliners. Check the lot numbers on the packaging; affected lots are 31504 and 31756. The product was manufactured by Quali Tech at 318 Hazel tine Drive, Chasma, MN 55318 USA.

  • Brand
    QualiTech
  • Category
    Food
FDA recall event · 18 products

All 18 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
Recall numberProduct, codes & lotsQuantity
F-0191-2017FI Dry Blueberry / Strawberry Blend, Product Code 21585. 40 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot: 3180040,080 lbs
F-0192-2017FE Carrot 281, Product Code 22281. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot: 31717, 3183240,150 lbs.
F-0193-2017FE Bacon 286, Product Code 22286. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot 31790400 lbs.
F-0194-2017FE Jalapeno 321A, Product Code 22321A. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lots: 31664, 31794, 319302,350 lbs.
F-0195-2017FE Green Bell Pepper 338, Product Code 22338. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot 31483300 lbs.
F-0196-2017FE RedBell Pepper 339, Product Code 22339. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot codes: 31476, 318026,000 lbs.
F-0197-2017FE Spinach 352, Product Code 22352. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lots: 31679, 319914,950 lbs.
F-0198-2017FE Cheddar Cheese, Product Code 22518. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lots: 31541, 31823, 31667, 318617,050 lbs.
F-0199-2017FE Red Bell Pepper, Product Code 22708. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lots: 31755, 320724,150 lbs.
F-0200-2017FE Jalapeno 709, Product Code 22709. 50 lb corrugated case with polyliner. Manufactured by: Quali Tech, 318 Hazel tine Drive, Chasma, MN 55318 USA; Lots: 31504, 317563,200 lbs.
F-0201-2017FE Rainbow Blend 714, Product Code 22714. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lots: 31584, 31665, 31841, 3184267,500 lbs.
F-0202-2017FE Green Bell Pepper, Product Code 22733. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lots: 31624, 319781.500 lbs.
F-0203-2017FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot: 31645, 31643400 lbs.
F-0204-2017FE Bacon, Product Code 22763. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot: 3175050 lbs.
F-0205-2017FE Rainbow Blend, Product Code 22795. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot: 319501,400 lbs.
F-0206-2017FE Bacon, Product Code 24117. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot: 31769500 lbs.
F-0207-2017FE Maple, Product Code 27128. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot: 31552, 31939, 3196932,750 lbs.
F-0208-2017PE Blueberry, Product Code 27136. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA; Lot: 31591, 31779, 31960176,900 lbs.
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume or distribute the recalled FE Jalapeno 709 due to potential E. coli contamination.

  2. Check lot numbers

    Verify if your product matches lots 31504 or 31756.

Where it went and when

Where it was distributed

Distributed in 10 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: yesIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Georgia, Idaho, Illinois, Indiana, Michigan, Minnesota, Texas, Washington.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

1. Firm started the recall: Jul 5, 201612. FDA classified it Class I: Oct 19, 201623. Published in FDA’s Enforcement Report: Oct 26, 201634. FDA terminated the recall: Sep 13, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Questions people ask

Where was this product sold?

It was distributed in AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA, and outside the US to include Canada.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0200-2017 (July 5, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0200-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA