Recall Register

Food recall: Baby Omega 3 Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.

Class III FDA enforcement event 72250. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable visual appearance standards for the product.

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

Zarbee's Naturals Inc. started this food recall on 21 Sep 2015. The firm address in the FDA record is in Draper, UT. FDA put the recall in Class III. FDA event 72250 has 2 product records. The first FDA enforcement report date is 13 Jul 2016. The record gives the status Terminated, with the termination date 17 Feb 2017.

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.

Nationwide to MN, IL, NJ and MI, further distributed nationwide. No foreign/VA/govt/military.

Recalling firm

Zarbee's Naturals Inc., Draper, UT.

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.

FDA event 72250: product records
Recall numberProductQuantityClassStatusReport date
F-1617-2016Baby Omega 3 Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.41,565 unitsClass IIITerminated13 Jul 2016
F-1618-2016Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.59,418 unitsClass IIITerminated13 Jul 2016

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 2015
607
Share of these events in Class III
7%
Product records in this event
2
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 72250. https://recallregister.com/fda/iii/72250/. 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: Nationwide to MN, IL, NJ and MI, further distributed nationwide. No foreign/VA/govt/military.
What quantity of product is in FDA event 72250?
The event has 2 product records. The first record gives this quantity: 41,565 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2015 have the same class?
7% of the 607 food events that started in 2015 are in Class III.