FDA Recall United States Terminated Historical recordClass II
Carfagnas Inc
- Product
- Carfagnas Spicy Chili Ready Sauce in 32 oz. glass jars.
- Published
- September 7, 2016
- Distribution
- Ohio only
Carfagnas Inc Recall: Acidified process not on file with the FDA
United States
TerminatedClass II
- Company
- Carfagnas Inc
- Product
- Carfagnas Mild Chili Ready Sauce in 32 oz. glass jars.
- Recall date
- May 3, 2016
- Terminated
- May 10, 2017
- Source
- FDA
Reason for recall
Acidified process not on file with the FDA
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Carfagnas Mild Chili Ready Sauce in 32 oz. glass jars. | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution
- Ohio only
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2014-2016
- Status
- Terminated
- Classification
- Class II
- Company
- Carfagnas Inc
- Product description
- Carfagnas Mild Chili Ready Sauce in 32 oz. glass jars.
- Quantity
- Not published in this source record
- Reason
- Acidified process not on file with the FDA
- Recall initiation date
- May 3, 2016
- Report date
- September 7, 2016
- Classification date
- Not published in this source record
- Termination date
- May 10, 2017
- Distribution pattern
- Ohio only
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Carfagnas Inc
Other recalls from Carfagnas 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 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?
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