Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 UPC 7 023672 414398 US $ 74.99 Sticker label: IKM IN
Summary
The FDA issued a Class I for Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 UPC 7 023672 by Lotus Mom Corporation dba Indian Kitchen Mart. Reason: Potential contamination with leachable lead..
Details
Source
Food Recall
External ID
H-0514-2026
Action Date
2026-02-25
Status
Ongoing
Category
food
Product Description
Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 UPC 7 023672 414398 US $ 74.99 Sticker label: IKM INDIAN KITCHEN MART
Lot/Code Info: UPC: 7 023672 414398
Quantity Affected: 9 units
Reason for Recall
Potential contamination with leachable lead.
Distribution
U.S. Distribution: CA, CO
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-21
Company
San Jose, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lotus Mom Corporation dba Indian Kitchen Mart has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lotus Mom Corporation dba Indian Kitchen Mart) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lotus Mom Corporation dba Indian Kitchen Mart have FDA actions?
Lotus Mom Corporation dba Indian Kitchen Mart has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0514-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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