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CriticalFDAfda-F-1693-2017CONTAMINATION

Strawberry Sorbet, 5 Liter, 1 unit/case

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
427
Recall Date
November 30, 2016
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1693-2017.

Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1693-2017.

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 Dolce Dolci Llc Dba Villa Dolce Gelato 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-1693-2017.

Dolce Dolci LLC dba Villa Dolce Gelato

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.

How to report to FDAFile a report at FDA

Dolce Dolci Llc Dba Villa Dolce Gelato Recall FAQ

Dolce Dolci Llc Dba Villa Dolce Gelato is the subject of a produce safety report: Strawberry Sorbet, 5 Liter, 1 unit/case. The notice was published on November 30, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 427 units are potentially affected.