Recall Register

Food recall: Meijer Caramel Corn, packed in 10 oz. bags, ( 283 g), 12 bags per case

Class II FDA enforcement event 72410. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Product labeling declared butter as an ingredient, but did not specify that the allergen milk is present in the product.

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

Meijer Distribution, Inc started this food recall on 7 Oct 2015. The firm address in the FDA record is in Grand Rapids, MI. FDA put the recall in Class II. FDA event 72410 has 1 product record. The first FDA enforcement report date is 2 Dec 2015. The record gives the status Terminated, with the termination date 29 Apr 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.

Domestic: MI, IN, OH, WI Foreign: None VA/DOD: None

Recalling firm

Meijer Distribution, Inc, Grand Rapids, MI.

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.

FDA event 72410: product records
Recall numberProductQuantityClassStatusReport date
F-0287-2016Meijer Caramel Corn, packed in 10 oz. bags, ( 283 g), 12 bags per case66,600 casesClass IITerminated2 Dec 2015

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 2015
607
Share of these events in Class II
46%
Product records in this event
1Median of the firm: 2
Events of the firm on the register
17

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 72410. https://recallregister.com/fda/ii/72410/. 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: Domestic: MI, IN, OH, WI Foreign: None VA/DOD: None
What quantity of product is in FDA event 72410?
The FDA record gives this quantity: 66,600 cases
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2015 have the same class?
46% of the 607 food events that started in 2015 are in Class II.