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Stop using now Food recall · FDA · Published June 30, 2016

Maglio Recalls Raw Cucumbers Due to Salmonella Risk

Maglio & Co recalls raw refrigerated cucumbers sold in Southern Valley due to Salmonella contamination. Check lot numbers and discard if affected.

🇺🇸 FDA recall #F-1921-2016FoodMaglio & Co Ready Fresh ›
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Recalling firmMaglio & Co Ready Fresh4287 N Port Washington Rd · Glendale, WI 53212
✎ GovInfoNow plain-language explainer

What happened, in plain English

Maglio & Co Ready Fresh is recalling raw refrigerated cucumbers because a sample tested positive for Salmonella spp. The product was distributed in corrugated cardboard cases under the Southern Valley brand. No specific remedy or return instructions are listed in this record. Read more at govinfonow.com/recall/23909-maglio-recalls-raw-cucumbers-due-to-salmonella-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/23909-maglio-recalls-raw-cucumbers-due-to-salmonella-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-1921-2016

Cite this page

“Maglio Recalls Raw Cucumbers Due to Salmonella Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23909-maglio-recalls-raw-cucumbers-due-to-salmonella-risk. Based on FDA recall #F-1921-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1921-2016%22&limit=1).

Why it’s dangerous

Salmonella bacteria can cause foodborne illness, leading to symptoms such as diarrhea, fever, and abdominal cramps. Because the product was raw, there was no cooking step to kill the bacteria before consumption.

Who’s affected

Consumers who purchased raw refrigerated cucumbers from Illinois, Wisconsin, Nebraska, Missouri, Michigan, and Minnesota between the relevant dates. Anyone who ate these cucumbers is at risk of Salmonella infection.

How to tell if you have this one

Look for raw refrigerated cucumbers in corrugated cardboard cases labeled 'Southern Valley Produce'. Check for Lot 16300705 and any of the following codes: X0882402, X0882328, X0882419, X0882663, X0882664, X0882776, X0882415, X0882808, X0035508, X0035548, X0035583, X0882379, X0882385, X0882465, X0882875, X0882585, X0882562, or X0882849.

  • Brand
    Maglio & Co Ready Fresh
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled cucumbers due to the risk of Salmonella contamination.

  2. Discard or return the item

    The record does not specify a remedy, so consumers should discard the product or contact the retailer for guidance.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: yesNEMissouri: yesMOKentucky: 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: “Il, WI, NE, MO, MI, MN .” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Michigan, Minnesota, Missouri, Nebraska, Wisconsin.

Recall timeline

FDA terminated this recall 13 months after the firm started it.

1. Firm started the recall: Jun 30, 201612. FDA classified it Class I: Aug 11, 201623. Published in FDA’s Enforcement Report: Aug 17, 201634. FDA terminated the recall: Jul 26, 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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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-1921-2016 (June 30, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1921-2016 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