Garland Ventures, LTD DBA Bally Plus Recall: Potential contamination with Listeria monocytogenes - F-1026-2020
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.
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 II mean?
FDA classifies this recall as Class II. 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
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of October 15, 2020.
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.