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Fannie May Confections Brands, Inc Recall: The products outer holiday wrap has an information panel that is incorrect. The information panel does not declare that pecans are in product. The actual box under wrapping correctly declares that pecans are in the product.

United States

TerminatedClass II

Company
Fannie May Confections Brands, Inc
Product
Fannie May Pixies , Caramel and Pecan Clusters covered in Mi…
Recall date
December 18, 2018
Terminated
April 28, 2020
Source
FDA

Reason for recall

The products outer holiday wrap has an information panel that is incorrect. The information panel does not declare that pecans are in product. The actual box under wrapping correctly declares that pecans are in the product.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Fannie May Pixies , Caramel and Pecan Clusters covered in Milk Chocolate 14 oz. Box - 12 units per case Not published in this source record 173,076 boxes (14 oz.) Pixies Lot numbers: 17352 1, 18262 2, 18263 2, 18291 1, 18291 2, 18293 2, 18295 2, 18298 2,18303 1, 18303 2, 18304 2, 18305 1, 18305 2, 18306 2, 18307 1, 18307 2, 18309 2,18310 1, 18310 2, 18311 2, 18312 2, 18313 2, 18316 1, 18316 2, 18317 2, 18318 1,18318 2, 18330 2, 18331 1

Distribution

  • The product at issue was distributed to customers in 10 states. IL
  • WI
  • IN
  • MN
  • WA
  • TX
  • PA
  • AL
  • KY
  • FL

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1315-2019
Event ID
81856
Status
Terminated
Classification
Class II
Company
Fannie May Confections Brands, Inc
Product description
Fannie May Pixies , Caramel and Pecan Clusters covered in Milk Chocolate 14 oz. Box - 12 units per case
Quantity
173,076 boxes (14 oz.) Pixies
Reason
The products outer holiday wrap has an information panel that is incorrect. The information panel does not declare that pecans are in product. The actual box under wrapping correctly declares that pecans are in the product.
Recall initiation date
December 18, 2018
Report date
May 8, 2019
Classification date
Not published in this source record
Termination date
April 28, 2020
Distribution pattern
The product at issue was distributed to customers in 10 states. IL, WI, IN,MN, WA, TX, PA, AL, KY, FL
UPC, lot, and code information
Lot numbers: 17352 1, 18262 2, 18263 2, 18291 1, 18291 2, 18293 2, 18295 2, 18298 2,18303 1, 18303 2, 18304 2, 18305 1, 18305 2, 18306 2, 18307 1, 18307 2, 18309 2,18310 1, 18310 2, 18311 2, 18312 2, 18313 2, 18316 1, 18316 2, 18317 2, 18318 1,18318 2, 18330 2, 18331 1
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Fannie May Confections Brands, Inc

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
Illinois 1
Wisconsin 1
Indiana 1
Minnesota 1
Washington 1
Texas 1
Pennsylvania 1
Alabama 1
Kentucky 1
Florida 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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.