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Lower risk Food recall · FDA · Published November 8, 2016

Prime Time Cucumbers Recall: Salmonella Contamination Risk

Prime Time International recalls fresh cucumbers due to potential Salmonella contamination. Consumers should check for tan cardboard cases with specific lot numbers and return affected products.

🇺🇸 FDA recall #F-0576-2017FoodPrime Time ›
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Recalling firmPrime Time International86705 Avenue 54 Ste A · Coachella, CA 92236-3814
✎ GovInfoNow plain-language explainer

What happened, in plain English

Prime Time International is recalling fresh cucumbers that may contain Salmonella bacteria. This contamination could cause foodborne illness if eaten, so affected products should be discarded or returned. Read more at govinfonow.com/recall/22915-prime-time-cucumbers-recall-salmonella-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/22915-prime-time-cucumbers-recall-salmonella-contamination-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-0576-2017

Cite this page

“Prime Time Cucumbers Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22915-prime-time-cucumbers-recall-salmonella-contamination-risk. Based on FDA recall #F-0576-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0576-2017%22&limit=1).

Why it’s dangerous

Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and stomach cramps. Contaminated cucumbers may be eaten without the user realizing they are unsafe.

Who’s affected

Anyone who purchased Prime Time's fresh cucumbers sold in tan cardboard cases with lot numbers 1-2885. People handling the cucumbers without proper food safety practices are at higher risk.

How to tell if you have this one

Check for cucumbers sold in tan cardboard cases with a red and green print. Look for lot numbers 1-2885 on the case or sticker.

  • Brand
    Prime Time
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for tan cardboard cases with red and green print and lot numbers 1-2885.

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: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew 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: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “CA, PA, AZ, OR” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Oregon, Pennsylvania.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Nov 8, 201612. FDA classified it Class I: Dec 6, 201623. Published in FDA’s Enforcement Report: Dec 14, 201634. FDA terminated the recall: Feb 9, 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-0576-2017 (November 8, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0576-2017 to see it in context.
  • Plain-language summary written by qwen3:4b 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