Class IIOngoingVoluntary: Firm initiated
INDIAN COOKWARE AND APPLIANCE LLC: food recall H-0349-2026
INDIAN COOKWARE AND APPLIANCE LLC of San Jose, CA recalled ALUMINIUM HAMMERED KADAI SIZE 7 8 901000 000057 MADE IN INDIA. Reason: Potential contamination due to leachable lead. The FDA listed it as Class II in its Enforcement Report dated Jan 7, 2026; distribution: California.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- ALUMINIUM HAMMERED KADAI SIZE 7 8 901000 000057 MADE IN INDIA
- Product quantity
- 10 pieces
- Reason for recall
- Potential contamination due to leachable lead.
- Codes, lots and dates on the package
- UPC: 8 901000 000057
- Distribution pattern
- U.S. Distribution: CA
- Recalling firm
- INDIAN COOKWARE AND APPLIANCE LLC, San Jose, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Oct 31, 2025 |
| Classified by the FDA | Dec 29, 2025 |
| Published in the Enforcement Report | Jan 7, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0349-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.