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Class I: serious health riskTerminated

Wm. E. Martin & Sons Chili Powder 50 Lbs Recall

CHILI POWDER 50 LBS

Wm. E. Martin & Sons Co., Inc. · Roslyn, NY

Risk level
Class I
Reported by FDA
Mar 18, 2015
Recall ID
F-1412-2015
Check your lot numberHow we source this data

Summary

Wm. E. Martin & Sons recalled Chili Powder 50 Lbs starting Jan 25, 2015. The FDA classified it as Class I (serious health risk) and published enforcement report F-1412-2015 on Mar 18, 2015. Reason: Cumin contains undeclared peanut protein. Status: Terminated.

Why it was recalled

Cumin contains undeclared peanut protein

Product description

CHILI POWDER 50 LBS

Lot numbers, UPCs & expiration codes

Lot Numbers: 1) M-56821, 2) M-56698

Where it was sold

CA, CT, FL, GA, IL, LA, MD, MS, NC, NH, NJ, NY, TX, VA

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-1412-2015
Classification
Class I
Status
Terminated
Recall initiated
Jan 25, 2015
FDA report date
Mar 18, 2015
Quantity
312 units
Recall type
Voluntary: Firm initiated
Recalling firm
Wm. E. Martin & Sons Co., Inc.

Original FDA data

Every field from FDA enforcement report F-1412-2015, exactly as published.

Show all FDA fields
City
Roslyn
State
NY
Status
Terminated
Country
United States
Event ID
70359
Address
55 Bryant Ave Ste 300
Code information
Lot Numbers: 1) M-56821, 2) M-56698
Postal code
11576-1158
Report date
Mar 18, 2015
Product type
Food
Recall number
F-1412-2015
Classification
Class I
Recalling firm
Wm. E. Martin & Sons Co., Inc.
Product quantity
312 units
Termination date
May 9, 2017
Reason for recall
Cumin contains undeclared peanut protein
Voluntary / mandated
Voluntary: Firm initiated
Product description
CHILI POWDER 50 LBS
Distribution pattern
CA, CT, FL, GA, IL, LA, MD, MS, NC, NH, NJ, NY, TX, VA
Recall initiation date
Jan 25, 2015
Initial firm notification
Letter
Center classification date
Mar 10, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1412-2015, published Mar 18, 2015. View the source record (openFDA) · FDA enforcement reports

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

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