Food recall: Product #4124: Caramel dip in plastic containers
Class II FDA enforcement event 66436. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
The firm received notification that the products were manufactured under insanitary conditions.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Gold Medal Products started this food recall on 24 Sep 2013. The firm address in the FDA record is in Cincinnati, OH. FDA put the recall in Class II. FDA event 66436 has 2 product records. The first FDA enforcement report date is 11 Dec 2013. The record gives the status Terminated, with the termination date 24 Dec 2013.
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.
The affected product was distributed in the following states: AK, AR, AZ, CA, CT, GA, IA, ID, IN, MA, MT, PA, TX & WI. The affected product was also distributed to Canada.
Recalling firm
Gold Medal Products, Cincinnati, OH.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
2 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0709-2014 | Product #4124: Caramel dip in plastic containers | 83 cases, with 4 containers per case | Class II | Terminated | 11 Dec 2013 |
| F-0710-2014 | Product #4123: Caramel dip in metal #10 containers | 50 case with 6 containers per case | Class II | Terminated | 11 Dec 2013 |
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 II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2013
- 546
- Share of these events in Class II
- 52%
- Product records in this event
- 2Median of the firm: 2
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 21 Mar 2014 | 2521 Cherry Glaze Pop (Flavoring for popcorn) - Paperboard Carton | Food | Class II | 4 |
| 21 Mar 2014 | 2372 HOT & SPICY; 4 pound plastic gallon containers; UPC 0 9093912372 7 | Food | Class III | 1 |
Official channels
- FDA enforcement report F-0709-2014The 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 66436. https://recallregister.com/fda/ii/66436/. 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:
The affected product was distributed in the following states: AK, AR, AZ, CA, CT, GA, IA, ID, IN, MA, MT, PA, TX & WI. The affected product was also distributed to Canada.
- What quantity of product is in FDA event 66436?
- The event has 2 product records. The first record gives this quantity:
83 cases, with 4 containers per case
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2013 have the same class?
- 52% of the 546 food events that started in 2013 are in Class II.