CLASS II Food recall · Reported 28 Aug 2024 · FDA Enforcement Report

Shahzada Pulses and Spices recalled by Advance Food International

Advance Food International is recalling Shahzada Pulses and Spices, distributed in Connecticut, Massachusetts, New Jersey, New York. The recall was initiated on 21 May 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNo codes.
Quantity recalled120 packets

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
F-1742-2024
FDA event ID
95044
Recalling firm
Advance Food International, Maspeth, NY
Classification
Class II
Status
Terminated
Recall initiated
21 May 2024
FDA classified
21 Aug 2024
Reported
28 Aug 2024
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Lead & Heavy Metals
Product category
Spices

Timeline

21 May 2024Recall initiated by company
21 Aug 2024Classified by FDA+92 days
28 Aug 2024Published 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

Product contains elevated levels of lead (2,030 ppb)

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

Shahzada brand Pulses and Spices; Cinnamon Powder; 7 oz (200g); packaged in clear plastic zip-top bags

Where it was distributed

NY, MA, NJ, CT

ConnecticutMassachusettsNew JerseyNew York

Questions about this recall

Why was it recalled?

Product contains elevated levels of lead (2,030 ppb)

Which lots are affected?

No codes.

Where was it sold?

NY, MA, NJ, CT

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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