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Unrated Food recall · FDA · Published February 17, 2017

Sunrise Growers Organic IQF Dark Sweet Cherries Recall: Possible Listeria Contamination

Sunrise Growers recalls 900 cartons of organic IQF Dark Sweet Cherries due to possible Listeria monocytogenes contamination. Consumers should avoid these products if they are affected.

🇺🇸 FDA recall #F-1562-2017FoodSunrise Growers ›
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Recalling firmSunrise Growers, Inc701 W Kimberly Ave · Placentia, CA 92870-6342
✎ GovInfoNow plain-language explainer

What happened, in plain English

Sunrise Growers is recalling organic IQF Dark Sweet Cherries because they may contain Listeria monocytogenes, a bacteria that can cause serious illness. This recall affects consumers who have purchased these cherries from the listed lots. Read more at govinfonow.com/recall/22214-sunrise-growers-organic-iqf-dark-sweet-cherries-recall-possible-listeria.

Source Summary by GovInfoNow · govinfonow.com/recall/22214-sunrise-growers-organic-iqf-dark-sweet-cherries-recall-possible-listeria · Updated October 8, 2026 · FDA enforcement record: FDA #F-1562-2017

Cite this page

“Sunrise Growers Organic IQF Dark Sweet Cherries Recall: Possible Listeria Contamination.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22214-sunrise-growers-organic-iqf-dark-sweet-cherries-recall-possible-listeria. Based on FDA recall #F-1562-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1562-2017%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacteria that can cause serious infections, especially in vulnerable populations like infants, pregnant women, and the elderly. Contaminated food can lead to illness if consumed, though the risk is not guaranteed for all consumers.

Who’s affected

Anyone who purchased Sunrise Growers organic IQF Dark Sweet Cherries from the recalled lots. Infants, pregnant women, and elderly individuals are at higher risk for serious illness from Listeria.

How to tell if you have this one

Check for cartons labeled with the lot numbers SWCB62071 PTR160495-28 or SWCB62072 PTR160495-28. These cherries were sold in 900 carton lots.

  • Brand
    Sunrise Growers
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Numbers

    Look for carton labels with lot numbers SWCB62071 PTR160495-28 or SWCB62072 PTR160495-28.

Where it went and when

Where it was distributed

Distributed in California.

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: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: 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: 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: “CA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: Feb 17, 201712. FDA classified it Class I: Mar 2, 201723. Published in FDA’s Enforcement Report: Mar 8, 201734. FDA terminated the recall: Jun 14, 201742017
  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-1562-2017 (February 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1562-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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