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Perfetti Van Melle USA Inc Recall: Blood was observed on equipment during packaging.

United States

TerminatedClass III

Company
Perfetti Van Melle USA Inc
Product
Airheads Mini Bars 12oz bags of assorted flavors. 12 - 12oz…
Recall date
September 2, 2016
Terminated
July 11, 2017
Source
FDA

Reason for recall

Blood was observed on equipment during packaging.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Airheads Mini Bars 12oz bags of assorted flavors. 12 - 12oz bags are included in cardboard cartons. Assorted flavors include Cherry, Watermelon, Blue Raspberry, and White Mystery. Not published in this source record 4,147 cases of 12/12oz bags On the cardboard cases: Lot codes 100061918 and 100063678 - On the retail bags: 61918 Best By 05-02-2018 and 63678 Best By 06-06-2018 - On individually wrapped candy pieces: 61469

Distribution

  • US Nationwide. The product was distributed to the following states: AL
  • CA
  • IL
  • IN
  • KY
  • LA
  • MD
  • ME
  • MI
  • MN
  • MO
  • NC
  • NE
  • NH
  • NJ
  • NY
  • OH
  • OK PA
  • SC
  • TX
  • VA
  • VT
  • WA
  • and WI.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0676-2017
Event ID
75112
Status
Terminated
Classification
Class III
Company
Perfetti Van Melle USA Inc
Product description
Airheads Mini Bars 12oz bags of assorted flavors. 12 - 12oz bags are included in cardboard cartons. Assorted flavors include Cherry, Watermelon, Blue Raspberry, and White Mystery.
Quantity
4,147 cases of 12/12oz bags
Reason
Blood was observed on equipment during packaging.
Recall initiation date
September 2, 2016
Report date
December 14, 2016
Classification date
Not published in this source record
Termination date
July 11, 2017
Distribution pattern
US Nationwide. The product was distributed to the following states: AL, CA, IL, IN, KY, LA, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NY, OH, OK PA, SC, TX, VA, VT, WA, and WI.
UPC, lot, and code information
On the cardboard cases: Lot codes 100061918 and 100063678 - On the retail bags: 61918 Best By 05-02-2018 and 63678 Best By 06-06-2018 - On individually wrapped candy pieces: 61469
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Perfetti Van Melle USA 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
Alabama 1
California 1
Illinois 1
Indiana 1
Kentucky 1
Louisiana 1
Maryland 1
Maine 1
Michigan 1
Minnesota 1
Missouri 1
North Carolina 1
Nebraska 1
New Hampshire 1
New Jersey 1
New York 1
Ohio 1
Oklahoma 1
Pennsylvania 1
South Carolina 1
Texas 1
Virginia 1
Vermont 1
Washington 1
Wisconsin 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 III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

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.