Severity
Low
Perfetti Van Melle USA Inc issued this FDA Food recall on December 14, 2016. Classified as Low severity (Class III). Approximately 4,147 cases of 12/12oz bags units are affected. The recall was issued because: Blood was observed on equipment during packaging.. This recall notice is sourced from official FDA Food enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
This FDA Food action (record #F-0676-2017) was formally reported on December 14, 2016, with the manufacturer initiating the action on September 2, 2016. It is classified under Low severity (Class III), with a current status of Terminated. Perfetti Van Melle USA Inc is listed as the recalling firm, operating out of Erlanger, KY. Federal records indicate 4,147 cases of 12/12oz bags units are affected, placing this recall in the million-unit bracket that typically triggers nationwide consumer alerts and retailer sweeps.
The documented reason for this recall is: Blood was observed on equipment during packaging. Distribution data in the federal record shows the product reached: 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.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 4 were also issued by FDA Food. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 10 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Severity
Low
Units Affected
4,147 cases of 12/12oz bags
Related Recalls
6
4 from same agency
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.
Blood was observed on equipment during packaging.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0676-2017 |
| Date reported | December 14, 2016 |
| Date initiated | September 2, 2016 |
| Recalling firm | Perfetti Van Melle USA Inc |
| Units affected | 4,147 cases of 12/12oz bags |
| 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. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
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Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
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Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).