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Stop using now Food recall · FDA · Published August 1, 2016

Odyssey Split Cooked King Crab Legs & Claws Recall: Listeria Contamination Risk

Odyssey Enterprises recalls Split Cooked King Crab Legs & Claws (UPC 28575 96323) due to Listeria monocytogenes contamination. Consumers should stop using and discard affected products immediately.

🇺🇸 FDA recall #F-2037-2016FoodOdyssey ›
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Recalling firmOdyssey Enterprises Inc2729 6th Ave S Ste 200 · Seattle, WA 98134-2101
✎ GovInfoNow plain-language explainer

What happened, in plain English

Odyssey Enterprises recalled Split Cooked King Crab Legs & Claws (20 lbs per box) because they were contaminated with Listeria monocytogenes. This bacteria can cause serious illness, so affected products must be discarded immediately. Read more at govinfonow.com/recall/23681-odyssey-split-cooked-king-crab-legs-claws-recall-listeria-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/23681-odyssey-split-cooked-king-crab-legs-claws-recall-listeria-contamination · Updated October 9, 2026 · FDA enforcement record: FDA #F-2037-2016

Cite this page

“Odyssey Split Cooked King Crab Legs & Claws Recall: Listeria Contamination Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23681-odyssey-split-cooked-king-crab-legs-claws-recall-listeria-contamination. Based on FDA recall #F-2037-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2037-2016%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacteria that can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. Contaminated crab products pose a risk of foodborne illness if eaten.

Who’s affected

Anyone who purchased Odyssey's Split Cooked King Crab Legs & Claws (UPC 28575 96323) from any retailer. People with weakened immune systems are at higher risk for severe illness.

How to tell if you have this one

Check for the UPC 28575 96323 on the label. The product is labeled as 'Split Cooked King Crab Leg & Claw' with a net weight of 20 lbs per box and instructions to keep frozen.

  • Brand
    Odyssey
  • Product
    Split Cooked King Crab Leg & Claw, repacked by Odyssey, net wt. 20 lbs. per box, keep frozen. UPC 28575 96323 The label
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Discard Product Immediately

    Remove and discard all affected Split Cooked King Crab Legs & Claws (UPC 28575 96323) from your freezer.

Where it went and when

Where it was distributed

Distributed in Wisconsin.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: 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: 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: “distributed in WI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Wisconsin.

Recall timeline

FDA terminated this recall 38 days after the firm started it.

1. Firm started the recall: Aug 1, 201612. FDA classified it Class II: Sep 8, 201623. FDA terminated the recall: Sep 8, 201634. Published in FDA’s Enforcement Report: Sep 14, 201642016
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-2037-2016 (August 1, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2037-2016 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