Monfitello Private Selection Peruvian Inspired Aji Recall

Why it was recalled

The firm was notified that the product may contain peanuts.

Product description

Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET WT 4 OZ (113g) INGREDIENTS: SOY SAUCE***CONTAINS: SOY. DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 MADE IN CANADA

Lot numbers, UPCs & expiration codes

Best By: MAR 20 2018. Lot # L213217/2A

Where it was sold

Products were shipped to the following states: AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NC, NE, NM, NV, OH, OR, SC, TN, TX, UT, VA, WA, WV & WY.

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-2373-2017
Classification: Class I
Status: Terminated
Recall initiated: May 26, 2017
FDA report date: Jun 28, 2017
Quantity: 384 cs/6/4 oz tubes
Recall type: Voluntary: Firm initiated
Recalling firm: Monfitello

Original FDA data

Every field from FDA enforcement report F-2373-2017, exactly as published.

Show all FDA fields

City: Lachine
Status: Terminated
Country: Canada
Event ID: 77412
Address: 2700 Jean-Baptiste-Deschamps Blvd
Code information: Best By: MAR 20 2018. Lot # L213217/2A
Report date: Jun 28, 2017
Product type: Food
Recall number: F-2373-2017
Classification: Class I
Recalling firm: Monfitello
Product quantity: 384 cs/6/4 oz tubes
Termination date: Apr 12, 2018
Reason for recall: The firm was notified that the product may contain peanuts.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET WT 4 OZ (113g) INGREDIENTS: SOY SAUCE***CONTAINS: SOY. DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 MADE IN CANADA
Distribution pattern: Products were shipped to the following states: AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NC, NE, NM, NV, OH, OR, SC, TN, TX, UT, VA, WA, WV & WY.
Recall initiation date: May 26, 2017
Initial firm notification: E-Mail
Center classification date: Jun 16, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2373-2017, published Jun 28, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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