CLASS II Food recall · Reported 22 Oct 2025 · FDA Enforcement Report
Silver Horse - Pure Aluminium recalled by Goyal Group
Goyal Group is recalling Silver Horse - Pure Aluminium, distributed in 13 states. The recall was initiated on 18 Sep 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-0058-2026
- FDA event ID
- 97599
- Recalling firm
- Goyal Group, Plainview, NY
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 18 Sep 2025
- FDA classified
- 15 Oct 2025
- Reported
- 22 Oct 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Lead & Heavy Metals
- Product category
- Milk
Timeline
| 18 Sep 2025 | Recall initiated by company | |
| 15 Oct 2025 | Classified by FDA | +27 days |
| 22 Oct 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Contains elevated levels of 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
1. SILVER HORSE - PURE ALUMINIUM MADE IN INDIA - ALUMINIUM MILK PAN 4 inches 2. SILVER HORSE - ALUMINIUM MATHAR KADAI - 26 inches
Where it was distributed
NY, NJ, MD, FL, PA, CO, CT, VA, NC, IL, TX, GA, MO
ColoradoConnecticutFloridaGeorgiaIllinoisMarylandMissouriNorth CarolinaNew JerseyNew YorkPennsylvaniaTexasVirginia
Questions about this recall
Why was it recalled?
Contains elevated levels of lead
Which lots are affected?
no codes
Where was it sold?
NY, NJ, MD, FL, PA, CO, CT, VA, NC, IL, TX, GA, MO
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 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.
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