Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN INDIA SIZE 5 Sticker label: $$24.99+TX
Summary
The FDA issued a Class II for Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN INDIA SIZE 5 Sticker by Lotus Mom Corporation dba Indian Kitchen Mart. Reason: Potential contamination with leachable lead..
Details
Source
Food Recall
External ID
H-0513-2026
Action Date
2026-02-25
Status
Ongoing
Category
food
Product Description
Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN INDIA SIZE 5 Sticker label: $$24.99+TX
Quantity Affected: 43 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 II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
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 II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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-0513-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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