CLASS II ONGOING Food recall · Reported 7 Jan 2026 · FDA Enforcement Report
Aluminium Hammered Kadai Size 7 recalled
Indian Cookware And Appliance is recalling Aluminium Hammered Kadai Size 7 8 901000 000057, distributed in California. The recall was initiated on 31 Oct 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0349-2026
- FDA event ID
- 97962
- Recalling firm
- Indian Cookware And Appliance, San Jose, CA
- Brand
- Aluminium Hammered
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 31 Oct 2025
- FDA classified
- 29 Dec 2025
- Reported
- 7 Jan 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Lead & Heavy Metals
- Product category
- Other
Timeline
| 31 Oct 2025 | Recall initiated by company | |
| 29 Dec 2025 | Classified by FDA | +59 days |
| 7 Jan 2026 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential contamination due to leachable lead.
Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.
Product as listed by the FDA
ALUMINIUM HAMMERED KADAI SIZE 7 8 901000 000057 MADE IN INDIA
Where it was distributed
U.S. Distribution: CA
Questions about this recall
Is Aluminium Hammered Kadai Size 7 8 901000 000057 recalled?
Yes. Indian Cookware And Appliance recalled Aluminium Hammered Kadai Size 7 8 901000 000057 on 31 Oct 2025. The recall is Class II and its status is Ongoing. Recall number H-0349-2026.
Why was it recalled?
Potential contamination due to leachable lead.
Which lots are affected?
UPC: 8 901000 000057
Where was it sold?
U.S. Distribution: CA
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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