Fresh Pak Fruit and Cheese Snacks Recall: Listeria Contamination Risk
Fresh Pak recalls 7oz Fruit and Cheese Snacks (UPC 7122817684) due to potential Listeria monocytogenes contamination. Affected lots: 312422, 312511, 312641, 312755, 312918. Use by dates Dec 17-21.
Recall notice
potentially been contaminated with Listeria monocytogenes
Contact the company
What happened, in plain English
Fresh Pak is recalling 7oz Fruit and Cheese Snacks that may contain Listeria monocytogenes, a bacteria that can cause serious illness. This recall affects products with specific lot numbers and use-by dates. Read more at govinfonow.com/recall/19905-fresh-pak-fruit-and-cheese-snacks-recall-listeria-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19905-fresh-pak-fruit-and-cheese-snacks-recall-listeria-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0612-2018
Cite this page
“Fresh Pak Fruit and Cheese Snacks Recall: Listeria Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19905-fresh-pak-fruit-and-cheese-snacks-recall-listeria-contamination-risk. Based on FDA recall #F-0612-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0612-2018%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause serious infections, especially in vulnerable groups like pregnant women, newborns, and the elderly. Contaminated food can lead to severe illness if consumed, though the risk depends on the amount eaten and individual health.
Who’s affected
Anyone who purchased Fresh Pak's 7oz Fruit and Cheese Snacks with the listed lot numbers or use-by dates. Infants, pregnant women, and elderly individuals are at higher risk for severe illness from Listeria.
How to tell if you have this one
Check the product label for lot numbers 312422, 312511, 312641, 312755, or 312918. The use-by date is between December 17 and 21. The UPC code is 7122817684.
- Brand
Fresh Pak- Product
7oz Fruit and cheese Snacks - no brand. 1 unit per case- Category
Food
All 6 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Michigan, Ohio and Wisconsin in retail stores and through distributors.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0607-2018 | 3lb Bag Dice Red Apples - no brand. 4 units per case; lots 312544,312807; no UPC; Use By Dec 29 - Jan 2. | 440 units |
| F-0608-2018 | 5/2.2oz Slice Apple Bags in clamshell - Aunt Mid s Michigan Apples brand. 6 units per case; lots 312547, 312806; UPC: 7122817430; Use By Dec 28 - Jan 1. | 2658 retail units |
| F-0609-2018 | 5/2.5oz Slice Apples w/ grapes bags in clamshell - Aunt Mid s brand. 6 units per case; lot 312546; UPC: 7122817431; Use By Dec 31. | 108 retail units |
| F-0610-2018 | 9oz Slice Apples Container - Fresh-Pak brand. 1 unit per case; lots 312447, 312537, 312666, 312780, 312943; UPC: 7122817686; Use By Dec 17 - 21. | 114 units |
| F-0611-2018 | 9oz Mix (red/green) Slice Apples Container - Fresh-Pak brand. 1 unit per case; lots 312448, 312538, 312781, 312944,312667; UPC: 7122817687; Use By Dec 17 - 21. | 121 units |
| F-0612-2018 | 7oz Fruit and cheese Snacks - no brand. 1 unit per case; lots 312422, 312511, 312641,312755, 312918; UPC: 7122817684; Use By Dec 17 - 21. | 160 units |
What to do — step by step
Check Product Label
Look for lot numbers 312422, 312511, 312641, 312755, or 312918 on the package.
Discard if Affected
If your product has one of the listed lot numbers, discard it immediately to avoid potential illness.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “Michigan, Ohio and Wisconsin in retail stores and through distributors.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Michigan, Ohio, Wisconsin.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0612-2018 (December 19, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0612-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.