FDA Recall United States TerminatedTerminated: October 18, 2018Historical recordClass I
Kellogg Company
- Product
- Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
- Published
- June 27, 2018
- Distribution
- Domestic: Alabama Arizona Arkansas Ca…
Kellogg Company Recall: Product contains sunflower seeds potentially contaminated with Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women. - F-1756-2016
United States
TerminatedClass I
- Company
- Kellogg Company
- Product
- Kashi Whole Grain Bars 35 g individual bar, 18 count reta…
- Recall date
- May 31, 2016
- Terminated
- November 17, 2016
- Source
- FDA
Reason for recall
Product contains sunflower seeds potentially contaminated with Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Kashi Whole Grain Bars 35 g individual bar, 18 count retail carton (630 g), 6 cartons per case | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution
- Nationwide
- Canada
- Bermuda
- Bahamas
- Gaum
- US Virgin Islands
- Mariana Islands
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1756-2016
- Status
- Terminated
- Classification
- Class I
- Company
- Kellogg Company
- Product description
- Kashi Whole Grain Bars 35 g individual bar, 18 count retail carton (630 g), 6 cartons per case
- Quantity
- Not published in this source record
- Reason
- Product contains sunflower seeds potentially contaminated with Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
- Recall initiation date
- May 31, 2016
- Report date
- July 27, 2016
- Classification date
- Not published in this source record
- Termination date
- November 17, 2016
- Distribution pattern
- Nationwide, Canada, Bermuda, Bahamas, Gaum, US Virgin Islands, Mariana Islands
- 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: Kellogg Company
Other recalls from Kellogg Company
FDA Recall United States TerminatedTerminated: March 24, 2017Historical recordClass II
Kellogg Company
- Product
- Kelloggs ¿ Eggo ¿ Nutri-Grain¿ Whole Wheat Waffles 12.3 o…
- Published
- October 19, 2016
- Distribution
- Multiple states
FDA Recall United States TerminatedTerminated: February 13, 2017Historical recordClass II
Kellogg Company
- Product
- Kellogg's Special K Mini Brownies Fudge, 6 ct, 4.44 oz.
- Published
- July 27, 2016
- Distribution
- Domestic: AL; AR; AZ; CA; CO; CT; FL; GA…
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.
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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.
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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 November 17, 2016.
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.
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