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Use caution Food recall · FDA · Published February 14, 2017

Good Plenty Supreme Abalone Noodles Recall: Undeclared Wheat

Lian Hwa Foods recalls Good Plenty Supreme Abalone Noodles due to undeclared wheat. Check expiration dates and serial numbers for details.

🇺🇸 FDA recall #F-1900-2017FoodGood Plenty ›
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Recalling firmLian Hwa Foods (USA) Inc.1500 Atlantic St · Union City, CA 94587-2006
✎ GovInfoNow plain-language explainer

What happened, in plain English

Lian Hwa Foods (USA) Inc. is recalling Good Plenty Brand Supreme Abalone Noodles because wheat was not properly declared on the product labeling. The noodles contain wheat, which poses a risk to individuals with wheat allergies or celiac disease. This recall involves approximately 200 boxes distributed in California. Read more at govinfonow.com/recall/22271-good-plenty-supreme-abalone-noodles-recall-undeclared-wheat.

Source Summary by GovInfoNow · govinfonow.com/recall/22271-good-plenty-supreme-abalone-noodles-recall-undeclared-wheat · Updated October 11, 2026 · FDA enforcement record: FDA #F-1900-2017

Cite this page

“Good Plenty Supreme Abalone Noodles Recall: Undeclared Wheat.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/22271-good-plenty-supreme-abalone-noodles-recall-undeclared-wheat. Based on FDA recall #F-1900-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1900-2017%22&limit=1).

Why it’s dangerous

The product label failed to declare wheat as an ingredient, even though wheat is present in the noodles. For individuals with severe wheat allergies or celiac disease, consuming undeclared wheat can trigger serious allergic reactions or other health issues.

Who’s affected

Consumers who purchased Good Plenty Brand Supreme Abalone Noodles, particularly those with wheat allergies or celiac disease, are at risk of an allergic reaction if they consume the product. The recall is limited to boxes distributed in California.

How to tell if you have this one

Check for Good Plenty Brand Supreme Abalone Noodles in a 21.2 oz. box containing a retort pouch of noodles and abalone. Verify the expiration date is 23/Dec./2017. For the noodle pack, look for serial numbers 1-238; for the abalone pack, look for serial numbers 1-217.

  • Brand
    Good Plenty
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify if your box matches the recalled description and has an expiration date of 23/Dec./2017 with the specific serial numbers listed.

  2. Stop Consumption

    Do not eat the noodles if they match the recalled criteria due to the undeclared wheat allergen.

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 only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Feb 14, 201712. FDA classified it Class III: Apr 7, 201723. Published in FDA’s Enforcement Report: Apr 19, 201734. FDA terminated the recall: May 1, 201742017
  1. Firm started the recall
  2. FDA classified it Class III
  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-1900-2017 (February 14, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1900-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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