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High RiskFDAfda-F-0819-2018OTHER

Flexfrost Protein Ice Cream Vanilla Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981

Category
Units Affected
2,927
Recall Date
January 11, 2018
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0819-2018.

The firm was notified by the Ohio Dept. of Agriculture (ODA) of insufficient pasteurization monitoring measures.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0819-2018.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Flexfrost or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0819-2018.

Flexfrost

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Flexfrost Recall FAQ

Flexfrost is the subject of a dairy safety report: Flexfrost Protein Ice Cream Vanilla Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981. The notice was published on January 11, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 2,927 units are potentially affected.