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CriticalFDAfda-F-0863-2022LISTERIA

All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice Cream Company; manufactured in Manchester, CT; all effected...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
90
Recall Date
February 1, 2022
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0863-2022.

Product may be contaminated with Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0863-2022.

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 The Royal Ice Cream Company Inc. 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-0863-2022.

The Royal Ice Cream Company Inc.

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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The Royal Ice Cream Company Inc. Recall FAQ

The Royal Ice Cream Company Inc. is the subject of a dairy safety report: All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice Cream Company; manufactured in Manchester, CT; all effected.... The notice was published on February 1, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 90 units are potentially affected.