CLASS I ONGOING Food recall · Reported 25 Feb 2026 · FDA Enforcement Report

Brass Pital Pot Sticker label: Brass Hammered Handi NO recalled

Lotus Mom is recalling Brass Pital Pot Sticker label: Brass Hammered Handi NO 3, distributed in California, Colorado. The recall was initiated on 21 Nov 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC: 7 023672 414398
Quantity recalled9 units

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-0514-2026
FDA event ID
98092
Recalling firm
Lotus Mom, San Jose, CA
Classification
Class I
Status
Ongoing
Recall initiated
21 Nov 2025
FDA classified
17 Feb 2026
Reported
25 Feb 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Lead & Heavy Metals
Product category
Bread

Timeline

21 Nov 2025Recall initiated by company
17 Feb 2026Classified by FDA+88 days
25 Feb 2026Published in enforcement report+8 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 with 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

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

Where it was distributed

U.S. Distribution: CA, CO

CaliforniaColorado

Questions about this recall

Why was it recalled?

Potential contamination with leachable lead.

Which lots are affected?

UPC: 7 023672 414398

Where was it sold?

U.S. Distribution: CA, CO

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 98092

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