Flexfrost Protein Ice Cream Mint Chip Recall: Insufficient Pasteurization Monitoring
Flexfrost recalls Protein Ice Cream Mint Chip due to insufficient pasteurization monitoring, potentially leading to food safety risks. Consumers should check product codes and contact the company for details.
Lower-risk recall
The firm was notified by the Ohio Dept. of Agriculture (ODA) of insufficient pasteurization monitoring measures.
Contact the company
What happened, in plain English
Flexfrost is recalling its Protein Ice Cream Mint Chip product because pasteurization monitoring was inadequate. This could pose food safety risks if the product wasn't properly pasteurized. Read more at govinfonow.com/recall/19808-flexfrost-protein-ice-cream-mint-chip-recall-insufficient-pasteurization-monitoring.
Source Summary by GovInfoNow · govinfonow.com/recall/19808-flexfrost-protein-ice-cream-mint-chip-recall-insufficient-pasteurization-monitoring · Updated October 7, 2026 · FDA enforcement record: FDA #F-0818-2018
Cite this page
“Flexfrost Protein Ice Cream Mint Chip Recall: Insufficient Pasteurization Monitoring.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19808-flexfrost-protein-ice-cream-mint-chip-recall-insufficient-pasteurization-monitoring. Based on FDA recall #F-0818-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0818-2018%22&limit=1).
Why it’s dangerous
The product was not properly pasteurized due to insufficient monitoring, which could lead to food safety risks. Pasteurization is a critical step to kill harmful bacteria in dairy products. Without it, the ice cream may contain pathogens that could cause illness.
Who’s affected
Anyone who purchased Flexfrost Protein Ice Cream Mint Chip from the company. Consumers most at risk are those who have the product and may have consumed it without proper pasteurization.
How to tell if you have this one
Check for the product code on the package, which is listed as SKU 1004. The product was sold with specific dates and is manufactured by Flexfrost in Whippany, NJ.
- Brand
Flexfrost- Category
Food
All 5 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 II- Status
Terminated- Distribution
Product was shipped to the following states: MA, MD,, MI, NC, NJ, NY, OH, PA & TN.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0815-2018 | Flexfrost Protein Ice Cream Chocolate Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981; SKU 1001 All Code Dates | 1200/4 oz cups |
| F-0816-2018 | Flexfrost Protein Ice Cream Cinnamon Chai Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981; SKU 1002 All Code Dates | 440/4 oz cups |
| F-0817-2018 | Flexfrost Protein Ice Cream Coffee Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981; SKU 1003 All Code Dates | 3120/4 oz cups |
| F-0818-2018 | Flexfrost Protein Ice Cream Mint Chip Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981; SKU 1004 All code Dates | 960/4 oz cups |
| F-0819-2018 | Flexfrost Protein Ice Cream Vanilla Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981; SKU 1005 All Code Dates | 2927/4 oz cups |
What to do — step by step
Check Product Code
Look for the SKU 1004 code on the package to identify the recalled product.
Where it went and when
Where it was distributed
Distributed in 9 states.
FDA distribution: “Product was shipped to the following states: MA, MD,, MI, NC, NJ, NY, OH, PA & TN.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Maryland, Massachusetts, Michigan, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Tennessee.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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-0818-2018 (January 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0818-2018 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.