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Stop using now Food recall · FDA · Published November 21, 2025

Indian Kitchen Mart Recalls Brass Pital Pot Due to Lead Risk

Indian Kitchen Mart recalls 9 units of its 4-quart Brass Pital Pot due to potential lead contamination. Check your UPC and lot details.

🇺🇸 FDA recall #H-0514-2026FoodIndian Kitchen Mart ›
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Contact the company

Recalling firmLotus Mom Corporation dba Indian Kitchen Mart945 Berryessa Rd Unit 5 · San Jose, CA 95133-1015
✎ GovInfoNow plain-language explainer

Lotus Mom Corporation, doing business as Indian Kitchen Mart, is recalling a small batch of its 4-quart Brass Pital Pot because the item may contain leachable lead. This specific recall involves only nine units distributed in California and Colorado. The record does not currently list a remedy or instructions for consumers. Read more at govinfonow.com/recall/6938-indian-kitchen-mart-recalls-brass-pital-pot-due-to-lead.

Source Summary by GovInfoNow · govinfonow.com/recall/6938-indian-kitchen-mart-recalls-brass-pital-pot-due-to-lead · Updated October 9, 2026 · Official notice: FDA #H-0514-2026

Cite this page

“Indian Kitchen Mart Recalls Brass Pital Pot Due to Lead Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6938-indian-kitchen-mart-recalls-brass-pital-pot-due-to-lead. Based on FDA recall #H-0514-2026.

The FDA announced on Nov. 21, 2025, that Lotus Mom Corporation dba Indian Kitchen Mart voluntarily recalled Brass Pital Pots due to potential lead contamination. Owners should contact the company for a refund. The agency issued recall number H-0514-2026.

How to tell if you have it

  • Brand: Indian Kitchen Mart
  • Product: Brass Pital Pot 4-quart
  • UPC: 7 023672 414398
  • Sticker label: BRASS HAMMERED HANDI NO 3
  • Sticker label: IKM INDIAN KITCHEN MART
  • Price: US $ 74.99

The hazard

The Brass Pital Pot poses a potential contamination risk from leachable lead, according to the FDA.

Context

GovInfoNow's records show Indian Kitchen Mart has been involved in other recent recalls of similar products, including India's Fine Foods 3B Cookware Recall on Oct. 28, 2025. Other recent recalls of similar products include Santos Brass Langri Cookware Recall (Nov. 12, 2025) and Sonex Aluminum Pot Recall (Nov. 19, 2025).

How to tell if you have this one

Look for a Brass Pital Pot with a capacity of 4 quarts. The item should have sticker labels reading "BRASS HAMMERED HANDI NO 3" and "IKM INDIAN KITCHEN MART." The UPC is 7 023672 414398, and the price tag shows US $ 74.99.

  • Brand
    Indian Kitchen Mart
  • Product
    Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 UPC 7 023672 414398 US $ 74.99 Sticker label: IKM
  • Category
    Food
FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Status
    Ongoing
  • Distribution
    U.S. Distribution: CA, CO
Recall numberProduct, codes & lotsQuantityClass
H-0511-2026IKM Aluminum Saucepan 9" with Wooden Handle. Sticker label: ALUMINIUM PAN 2 SIDE POUTED WOODEN HANDLE 9" UPC 7 023672 411878 US $ 17.99 Sticker label: IKM INDIAN KITCHEN MART; UPC: 7 023672 41187856 unitsClass II
H-0512-2026Brass Tope. Sticker label: $29.99+TAX10 unitsClass II
H-0513-2026Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN INDIA SIZE 5 Sticker label: $$24.99+TX43 unitsClass II
H-0514-2026Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 UPC 7 023672 414398 US $ 74.99 Sticker label: IKM INDIAN KITCHEN MART; UPC: 7 023672 4143989 unitsClass I
Based on the official FDA remedy

What to do — step by step

  1. Stop using the pot

    Do not use the recalled Brass Pital Pot for cooking or storing food due to the risk of lead contamination.

  2. Check your product details

    Verify if you own the item by checking for the specific UPC 7 023672 414398 and the "BRASS HAMMERED HANDI NO 3" label.

  3. Monitor for updates

    Since no remedy is currently stated in the record, check official sources for further instructions on returns or refunds.

Where it went and when

Where it was distributed

Distributed in California and Colorado.

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: yesCONebraska: 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: “U.S. Distribution: CA, CO” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Colorado.

Recall timeline

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

1. Firm started the recall: Nov 21, 202512. FDA classified it Class I: Feb 17, 202623. Published in FDA’s Enforcement Report: Feb 25, 2026320252026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Where was this product sold?

The record states distribution occurred in the U.S., specifically in California and Colorado.

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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 #H-0514-2026 (November 21, 2025)
  • Plain-language summary written by qwen3.6:35b-a3b 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