Garland Ventures, LTD DBA Bally Plus Recall: Potential contamination with Listeria monocytogenes
United States
TerminatedClass II
- Company
- Garland Ventures, LTD DBA Bally Plus
- Product
- Freshness Guaranteed Five Cheese Stuffed Shells Traditional…
- Recall date
- June 29, 2020
- Terminated
- October 15, 2020
- Source
- FDA
Reason for recall
Potential contamination with Listeria monocytogenes
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Freshness Guaranteed Five Cheese Stuffed Shells Traditional Italian Ricotta Filled Shells with Marinara Sauce 10.76 ounces UPC 7874235174 | 7874235174 | 1095 cases | lot# F080SS and F090SS |
Distribution
- Nationwide throughout the US
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1026-2020
- Event ID
- 85953
- Status
- Terminated
- Classification
- Class II
- Company
- Garland Ventures, LTD DBA Bally Plus
- Product description
- Freshness Guaranteed Five Cheese Stuffed Shells Traditional Italian Ricotta Filled Shells with Marinara Sauce 10.76 ounces UPC 7874235174
- Quantity
- 1095 cases
- Reason
- Potential contamination with Listeria monocytogenes
- Recall initiation date
- June 29, 2020
- Report date
- July 22, 2020
- Classification date
- Not published in this source record
- Termination date
- October 15, 2020
- Distribution pattern
- Nationwide throughout the US
- UPC, lot, and code information
- UPC 7874235174; lot# F080SS and F090SS
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Garland Ventures, LTD DBA Bally Plus
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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
