Food recall: Individually 2/3 oz. slices of American cheese product individually wrapped in transparent plastic an packaged in 12…
Class III FDA enforcement event 69142. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Kraft Foods Group is voluntarily recalling 7,691 cases of select varieties of regular Kraft American Singles Pasteurized Prepared Cheese Product. A supplier did not store an ingredient used in this product in accordance with Kraft's temperature standards.
Class III, in the words of FDA
a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences
Kraft Heinz Foods started this food recall on 29 Aug 2014. The firm address in the FDA record is in Northfield, IL. FDA put the recall in Class III. FDA event 69142 has 1 product record. The first FDA enforcement report date is 22 Oct 2014. The record gives the status Terminated, with the termination date 8 Aug 2016.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
US: Nationwide (AL, AR, CA, CA, FL, GA, IL, IN, KS, MI, NC, NJ, OH, OK, TN, TX, VA)
Recalling firm
Kraft Heinz Foods, Northfield, IL.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
1 product record in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0022-2015 | Individually 2/3 oz. slices of American cheese product individually wrapped in transparent plastic an packaged in 12 oz. and 16 oz.. packages, and 4 lb. cartons under the Kraft brand name. Cases of 12 oz. packages include 48 packages per case. Cases of 16 oz. packages include either 12 or 36 packages per case. Cases… | 7,691 cases | Class III | Terminated | 22 Oct 2014 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class III: The lowest of the three FDA recall classes.
The event in context
- Food events that started in 2014
- 573
- Share of these events in Class III
- 9%
- Product records in this event
- 1Median of the firm: 2
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 29 Dec 2015 | CapriSun fruit punch roarin'waters packaged in a blue and white box with pictures of fruit and white lettering. | Food | Class II | 6 |
| 31 Jul 2015 | Kraft American Singles Pasteurized prepared cheese products packaged clear plastic. Sold at retail as 1 lb. packages. So | Food | Class II | 2 |
Official channels
- FDA enforcement report F-0022-2015The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 69142. https://recallregister.com/fda/iii/69142/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
US: Nationwide (AL, AR, CA, CA, FL, GA, IL, IN, KS, MI, NC, NJ, OH, OK, TN, TX, VA)
- What quantity of product is in FDA event 69142?
- The FDA record gives this quantity:
7,691 cases
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2014 have the same class?
- 9% of the 573 food events that started in 2014 are in Class III.