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Lower risk Food recall · FDA · Published August 3, 2017

Go Fresh VEG MIX BROC/RED-ON-PEP STRIP Recall: E. coli O26 Contamination Risk

Go Fresh recalls VEG MIX BROC/RED-ON-PEP STRIP (2/5#) with lot codes 130213 and 130214 due to potential E. coli O26 contamination. Consumers should check their products and contact the manufacturer for details.

🇺🇸 FDA recall #F-3414-2017FoodGo Fresh ›
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Recalling firmGo Fresh2521 E Hennepin Ave · Minneapolis, MN 55413-2911
✎ GovInfoNow plain-language explainer

What happened, in plain English

Go Fresh is recalling a specific broccoli and pepper mix product because it may contain harmful E. coli O26 bacteria. This contamination could cause foodborne illness if the product is consumed. Read more at govinfonow.com/recall/20572-go-fresh-veg-mix-broc-red-on-pep-strip-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/20572-go-fresh-veg-mix-broc-red-on-pep-strip-recall · Updated October 7, 2026 · FDA enforcement record: FDA #F-3414-2017

Cite this page

“Go Fresh VEG MIX BROC/RED-ON-PEP STRIP Recall: E. coli O26 Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20572-go-fresh-veg-mix-broc-red-on-pep-strip-recall. Based on FDA recall #F-3414-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3414-2017%22&limit=1).

Why it’s dangerous

The product may be contaminated with E. coli O26 bacteria, which can cause food poisoning. This bacteria is typically spread through contaminated food and can lead to symptoms like diarrhea, vomiting, and fever.

Who’s affected

Anyone who purchased the Go Fresh VEG MIX BROC/RED-ON-PEP STRIP (2/5#) with lot codes 130213 or 130214. People who eat the product are at risk of foodborne illness.

How to tell if you have this one

Check the lot code on the product label. The affected items have lot codes 130213 or 130214. The product is a 2/5# broccoli and pepper mix sold by Go Fresh.

  • Brand
    Go Fresh
  • Category
    Food
FDA recall event · 3 products

All 3 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 II
  • Status
    Terminated
  • Distribution
    5 distributers in 4 states: MN, WI, IA, and ND.
Recall numberProduct, codes & lots
F-3412-2017Broccoli Florets packaged with the following [Product Brand, amount per case / pounds per package, item code]: 1) Imperial Fresh, 1/5#, 6712509; 2) Imperial Fresh, 1/3#, 9731258; 3) Imperial Fresh, 1/5#, 1515360; 4) SYSCO Imperial, 4/3#, 6540843; 5) Imperial Fresh, 1/5#, 6709356; 6) SYSCO Imperial, 4/3#, 6540843; Lot codes: 130213 and 130214
F-3413-2017Imperial Fresh Veg Blend 7-Way, 2/5#, 7512033; Lot codes: 130213 and 130214
F-3414-2017US Foods VEG MIX BROC/RED-ON-PEP STRIP, 2/5#, 8651259; Lot codes: 130213 and 130214
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Code

    Look for lot codes 130213 or 130214 on the product label to identify affected items.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: yesNDMinnesota: yesMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew 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: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “5 distributers in 4 states: MN, WI, IA, and ND.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Iowa, Minnesota, North Dakota, Wisconsin.

Recall timeline

FDA terminated this recall 47 days after the firm started it.

1. Firm started the recall: Aug 3, 201712. FDA classified it Class II: Aug 22, 201723. Published in FDA’s Enforcement Report: Aug 30, 201734. FDA terminated the recall: Sep 19, 201742017
  1. Firm started the recall
  2. FDA classified it Class II
  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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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-3414-2017 (August 3, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3414-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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