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Use caution Food recall · FDA · Published October 30, 2018

The Perfect Bite Co. Recalls Quinoa Blend Due to Undeclared Wheat

The Perfect Bite Co. recalls Southwest Style Vegetable & Quinoa Protein Blend because wheat is undeclared on the label, posing a risk to those with allergies.

🇺🇸 FDA recall #F-0629-2019FoodThe Perfect Bite Co. ›
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Recalling firmThe Perfect Bite Co.747 W Wilson Ave · Glendale, CA 91203-2447
✎ GovInfoNow plain-language explainer

What happened, in plain English

The Perfect Bite Co. is recalling Southwest Style Vegetable & Quinoa Protein Blend because the product contains farro but does not list wheat as an ingredient on the label. Although quinoa was listed in the name, the product actually contained farro and brown rice. This undeclared allergen poses a risk to consumers with wheat allergies or celiac disease. Read more at govinfonow.com/recall/18206-the-perfect-bite-co-recalls-quinoa-blend-due-to-undeclared.

Source Summary by GovInfoNow · govinfonow.com/recall/18206-the-perfect-bite-co-recalls-quinoa-blend-due-to-undeclared · Updated October 11, 2026 · FDA enforcement record: FDA #F-0629-2019

Cite this page

“The Perfect Bite Co. Recalls Quinoa Blend Due to Undeclared Wheat.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18206-the-perfect-bite-co-recalls-quinoa-blend-due-to-undeclared. Based on FDA recall #F-0629-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0629-2019%22&limit=1).

Why it’s dangerous

The product label failed to declare wheat, which is present because the main grain ingredient is farro (a type of wheat). For individuals with wheat allergies or celiac disease, consuming undeclared wheat can trigger serious allergic reactions or digestive distress.

Who’s affected

Consumers who purchased the recalled frozen vegetable blend, particularly those with wheat allergies or celiac disease, are at risk of an allergic reaction. The product was distributed in Massachusetts, Maryland, and Pennsylvania.

How to tell if you have this one

Check your freezer for Southwest Style Vegetable & Quinoa Protein Blend distributed by Foodhold USA LLC. Look for the lot codes R15602 or R15862 and an expiration date of 10.2.2020 on the packaging.

  • Brand
    The Perfect Bite Co.
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if your package matches the recalled lot codes R15602 or R15862 with expiration date 10.2.2020.

  2. Avoid Consumption

    Do not eat the product if you have a wheat allergy due to the undeclared wheat ingredient.

Where it went and when

Where it was distributed

Distributed in 3 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: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: 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: “MA, MD, PA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland, Massachusetts, Pennsylvania.

Recall timeline

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

1. Firm started the recall: Oct 30, 201812. FDA classified it Class II: Nov 16, 201823. Published in FDA’s Enforcement Report: Nov 28, 201834. FDA terminated the recall: Jan 29, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class II
  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-0629-2019 (October 30, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0629-2019 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