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Lower risk Food recall · FDA · Published May 11, 2021

Mideo's Marinara Glass Jars Recall: Incorrect Potassium Labeling

RC Industries Inc. recalls Mideo's Marinara Glass 32oz jars due to incorrect potassium labeling on servings. Affected jars have specific batch numbers and product codes. Consumers should check labels for the listed batches.

🇺🇸 FDA recall #F-0661-2021FoodMideo's ›
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Recalling firmRC Industries Inc.620 Main St N · Navarre, OH 44662-8556
✎ GovInfoNow plain-language explainer

What happened, in plain English

RC Industries Inc. is recalling Mideo's Marinara Glass 32oz jars because the potassium content per serving on the label is incorrect. This labeling error could lead to confusion about the product's nutritional information, but it does not pose a safety risk to consumers. Read more at govinfonow.com/recall/14540-mideo-s-marinara-glass-jars-recall-incorrect-potassium-labeling.

Source Summary by GovInfoNow · govinfonow.com/recall/14540-mideo-s-marinara-glass-jars-recall-incorrect-potassium-labeling · Updated October 4, 2026 · FDA enforcement record: FDA #F-0661-2021

Cite this page

“Mideo's Marinara Glass Jars Recall: Incorrect Potassium Labeling.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14540-mideo-s-marinara-glass-jars-recall-incorrect-potassium-labeling. Based on FDA recall #F-0661-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0661-2021%22&limit=1).

Why it’s dangerous

The recall is due to an incorrect potassium content listed per serving on the product label. This labeling error means the nutritional information may not match the actual product, potentially causing confusion for consumers tracking their potassium intake. However, the error does not involve physical harm or safety risks.

Who’s affected

Anyone who owns or uses Mideo's Marinara Glass 32oz jars with the listed batch numbers or product code 7234300021. People most at risk are those who rely on accurate nutritional labeling for dietary planning.

How to tell if you have this one

Check the jar's label for batch numbers: 041423A through 040523C, 032623A through 032723B, 022523C through 011323C, or product number 7234300021. The jars come in sets of six per case.

  • Brand
    Mideo's
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label for Batch Number

    Look for batch numbers on the jar label: 041423A, 041423B, 041423C, 040523A, 040523B, 040523C, 032623A, 032723A, 032723B, 022523C, 022223C, 021523C, 020923A, 020823C, 011423C, 011423B, 011423A, 011323A, 011323B, or 011323C.

Where it went and when

Where it was distributed

Distributed in 9 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew 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: yesTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “FL, GA, MI, NY, NC, OH, PA, TN, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, Georgia, Michigan, New York, North Carolina, Ohio, Pennsylvania, Tennessee, Wisconsin.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: May 11, 202112. FDA classified it Class II: Jun 8, 202123. Published in FDA’s Enforcement Report: Jun 16, 202134. FDA terminated the recall: Nov 8, 202142021
  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.

✎ GovInfoNow

Questions people ask

Do I need to stop using these jars?

No, the recall is for labeling accuracy, not safety. You can continue using the jars but should check the label for the correct batch numbers if you need to verify the product.

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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-0661-2021 (May 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0661-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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