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Class II: temporary or reversible health riskOngoing

Lotus Mom Corporation dba Indian Kitchen Mart Brass Tope Recall

Brass Tope

Lotus Mom Corporation dba Indian Kitchen Mart · San Jose, CA

Risk level
Class II
Reported by FDA
Feb 25, 2026
Recall ID
H-0512-2026
Check your lot numberHow we source this data

Summary

Lotus Mom Corporation dba Indian Kitchen Mart recalled Brass Tope starting Nov 21, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0512-2026 on Feb 25, 2026. Reason: Potential contamination with leachable lead. Status: Ongoing.

Why it was recalled

Potential contamination with leachable lead.

Product description

Brass Tope. Sticker label: $29.99+TAX

Lot numbers, UPCs & expiration codes

No codes were listed in the FDA report.

Where it was sold

U.S. Distribution: CA, CO

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0512-2026
Classification
Class II
Status
Ongoing
Recall initiated
Nov 21, 2025
FDA report date
Feb 25, 2026
Quantity
10 units
Recall type
Voluntary: Firm initiated
Recalling firm
Lotus Mom Corporation dba Indian Kitchen Mart

Original FDA data

Every field from FDA enforcement report H-0512-2026, exactly as published.

Show all FDA fields
City
San Jose
State
CA
Status
Ongoing
Country
United States
Event ID
98092
Address
945 Berryessa Rd Unit 5
Postal code
95133-1015
Report date
Feb 25, 2026
Product type
Food
Recall number
H-0512-2026
Classification
Class II
Recalling firm
Lotus Mom Corporation dba Indian Kitchen Mart
Product quantity
10 units
Reason for recall
Potential contamination with leachable lead.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Brass Tope. Sticker label: $29.99+TAX
Distribution pattern
U.S. Distribution: CA, CO
Recall initiation date
Nov 21, 2025
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Feb 17, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0512-2026, published Feb 25, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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