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Monfitello Recall: The firm was notified that the product may contain peanuts.

United States

TerminatedClass I

Company
Monfitello
Product
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINA…
Recall date
May 26, 2017
Terminated
April 12, 2018
Source
FDA

Reason for recall

The firm was notified that the product may contain peanuts.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 MADE IN CANADA Not published in this source record 3,244 cs/6/4 oz tubes Best By: MAR 23 2018, Lot #'s: L209317/1A, L209417/1A, L212817/1A, L213217/1A

Distribution

  • 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.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2372-2017
Event ID
77412
Status
Terminated
Classification
Class I
Company
Monfitello
Product description
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 MADE IN CANADA
Quantity
3,244 cs/6/4 oz tubes
Reason
The firm was notified that the product may contain peanuts.
Recall initiation date
May 26, 2017
Report date
June 28, 2017
Classification date
Not published in this source record
Termination date
April 12, 2018
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.
UPC, lot, and code information
Best By: MAR 23 2018, Lot #'s: L209317/1A, L209417/1A, L212817/1A, L213217/1A
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 77412 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Monfitello

Product
Private Selection Peruvian Inspired Aji Amarillo Culinary Sp…
Published
June 28, 2017
Distribution
Products were shipped to the following s…

View recall →

Responsible company: Monfitello

Other recalls from Monfitello

FDA Recall United States Terminated Historical recordClass I

Monfitello

Product
Private Selection Peruvian Inspired Aji Amarillo Culinary Sp…
Published
June 28, 2017
Distribution
Products were shipped to the following s…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Alaska 1
Alabama 1
Arkansas 1
Arizona 1
California 1
Colorado 1
Georgia 1
Idaho 1
Illinois 1
Indiana 1
Kansas 1
Kentucky 1
Louisiana 1
Michigan 1
Missouri 1
Mississippi 1
Montana 1
North Carolina 1
Nebraska 1
New Mexico 1
Nevada 1
Ohio 1
Oregon 1
South Carolina 1
Tennessee 1
Texas 1
Utah 1
Virginia 1
Washington 1
West Virginia 1
Wyoming 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.