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Class III: unlikely to cause harmTerminated

Nicomex Tequesquite Recall

Nicomex Tequesquite

Nicomex Inc. · Passaic, NJ

Risk level
Class III
Reported by FDA
Apr 17, 2024
Recall ID
F-1121-2024
Check your lot numberHow we source this data

Summary

Nicomex recalled Nicomex Tequesquite starting Feb 15, 2024. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1121-2024 on Apr 17, 2024. Reason: Elevated lead levels. Status: Terminated.

Why it was recalled

Elevated lead levels

Product description

Nicomex Tequesquite, Net Wt. 1.5oz (42.52gms), UPC: 8 8467810180 7. Packaged in a plastic bag.

Lot numbers, UPCs & expiration codes

N/A

Where it was sold

Distributed to distributors in NJ, then further distributed to retail stores in NJ and NY.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1121-2024
Classification
Class III
Status
Terminated
Recall initiated
Feb 15, 2024
FDA report date
Apr 17, 2024
Quantity
Approximately 192 units
Recall type
Voluntary: Firm initiated
Recalling firm
Nicomex Inc.

Original FDA data

Every field from FDA enforcement report F-1121-2024, exactly as published.

Show all FDA fields
City
Passaic
State
NJ
Status
Terminated
Country
United States
Event ID
94093
Address
19 Wall St
Postal code
07055-8346
Report date
Apr 17, 2024
Product type
Food
Recall number
F-1121-2024
Classification
Class III
Recalling firm
Nicomex Inc.
Product quantity
Approximately 192 units
Termination date
Feb 26, 2025
Reason for recall
Elevated lead levels
Voluntary / mandated
Voluntary: Firm initiated
Product description
Nicomex Tequesquite, Net Wt. 1.5oz (42.52gms), UPC: 8 8467810180 7. Packaged in a plastic bag.
Distribution pattern
Distributed to distributors in NJ, then further distributed to retail stores in NJ and NY.
Recall initiation date
Feb 15, 2024
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 8, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1121-2024, published Apr 17, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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