FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass I
Dolce Dolci LLC dba Villa Dolce Gelato
- Product
- Strawberry Sorbet, 5 Liter, 1 unit/case
- Published
- March 29, 2017
- Distribution
- Nationwide
Dolce Dolci LLC dba Villa Dolce Gelato Recall: Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus. - F-1692-2017
United States
TerminatedClass I
- Company
- Dolce Dolci LLC dba Villa Dolce Gelato
- Product
- Strawberry Gelato, 5 Liter, 1 unit/case
- Recall date
- November 30, 2016
- Terminated
- May 1, 2017
- Source
- FDA
Reason for recall
Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Strawberry Gelato, 5 Liter, 1 unit/case | Not published in this source record | 602 units | Exp. Date Feb 5, 2018 Exp. Date March 19, 2018 |
Distribution
- Nationwide in US: OK
- CA
- NV
- MD
- CA
- FL
- MA
- NY
- CO
- AZ
- SC
- MN
- ND
- UT
- MT
- IL
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1692-2017
- Event ID
- 75861
- Status
- Terminated
- Classification
- Class I
- Company
- Dolce Dolci LLC dba Villa Dolce Gelato
- Product description
- Strawberry Gelato, 5 Liter, 1 unit/case
- Quantity
- 602 units
- Reason
- Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.
- Recall initiation date
- November 30, 2016
- Report date
- March 29, 2017
- Classification date
- Not published in this source record
- Termination date
- May 1, 2017
- Distribution pattern
- Nationwide in US: OK, CA, NV, MD, CA, FL, MA, NY, CO, AZ, SC, MN, ND, UT, MT, IL
- UPC, lot, and code information
- Exp. Date Feb 5, 2018 Exp. Date March 19, 2018
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 75861 with 1 other product entry in Public Health Trace.
Responsible company: Dolce Dolci LLC dba Villa Dolce Gelato
Other recalls from Dolce Dolci LLC dba Villa Dolce Gelato
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass I
Dolce Dolci LLC dba Villa Dolce Gelato
- Product
- Strawberry Sorbet, 5 Liter, 1 unit/case
- Published
- March 29, 2017
- Distribution
- Nationwide
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Oklahoma | 1 |
| California | 1 |
| Nevada | 1 |
| Maryland | 1 |
| Florida | 1 |
| Massachusetts | 1 |
| New York | 1 |
| Colorado | 1 |
| Arizona | 1 |
| South Carolina | 1 |
| Minnesota | 1 |
| North Dakota | 1 |
| Utah | 1 |
| Montana | 1 |
| Illinois | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of May 1, 2017.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.