FDA Recall United States Terminated Historical recordClass III
LiDestri Foods, Inc.
- Product
- Wegmans ITALIAN CLASSICS Organic BLUSH SAUCE, NET WT 23.5 OZ…
- Published
- October 19, 2016
- Distribution
- PA thru Wegmans markets
LiDestri Foods, Inc. Recall: Product may contain undeclared fish.
United States
TerminatedClass I
- Company
- LiDestri Foods, Inc.
- Product
- Wegmans Italian Classics Diavolo Pasta Sauce 24 OZ
- Recall date
- May 16, 2023
- Terminated
- August 4, 2023
- Source
- FDA
Reason for recall
Product may contain undeclared fish.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Wegmans Italian Classics Diavolo Pasta Sauce 24 OZ | Not published in this source record | 623 cases | UPC: 077890222409 Lot Code #F0589 Best By 3/31/25 |
Distribution
- Delaware
- District of Columbia
- Maryland
- Massachusetts
- New Jersey
- New York
- North Carolina
- Pennsylvania
- and Virginia
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0993-2023
- Event ID
- 92354
- Status
- Terminated
- Classification
- Class I
- Company
- LiDestri Foods, Inc.
- Product description
- Wegmans Italian Classics Diavolo Pasta Sauce 24 OZ
- Quantity
- 623 cases
- Reason
- Product may contain undeclared fish.
- Recall initiation date
- May 16, 2023
- Report date
- June 28, 2023
- Classification date
- Not published in this source record
- Termination date
- August 4, 2023
- Distribution pattern
- Delaware, District of Columbia, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, and Virginia
- UPC, lot, and code information
- UPC: 077890222409 Lot Code #F0589 Best By 3/31/25
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: LiDestri Foods, Inc.
Other recalls from LiDestri Foods, Inc.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
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?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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.
