Severity
Low
LowClass IIITerminated
FDA Food recall · Reported July 13, 2016
Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable visual appearance standards for the product.
Zarbee's Naturals Inc. recalled Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with … - a low-severity action.
Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with … was recalled by Zarbee's Naturals Inc. in July 13, 2016. Reason: Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable vis…. Check the official notice for the remedy. Verify recall #F-1618-2016 with the FDA Food before acting.
The recall
Zarbee's Naturals Inc. issued this low-severity FDA Food recall-Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable vis….
- Low
- severity level
- 59K units
- affected scope
- Class III
- classification
- July 13, 2016
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1618-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1618-2016) was formally reported on July 13, 2016, with the manufacturer initiating the action on September 21, 2015. It is classified under Low severity (Class III), with a current status of Terminated. Zarbee's Naturals Inc. is listed as the recalling firm, operating out of Draper, UT. Federal records list the affected scope as 59,418 units.
The documented reason for this recall is: Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable visual appearance standards for the product. Distribution data in the federal record shows the product reached: Nationwide to MN, IL, NJ and MI, further distributed nationwide. No foreign/VA/govt/military.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
59,418 units
Related Recalls
6
0 from same agency
Product description
Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
Reason for recall
Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable visual appearance standards for the product.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-1618-2016 |
| Date reported | July 13, 2016 |
| Date initiated | September 21, 2015 |
| Recalling firm | Zarbee's Naturals Inc. |
| Firm location | Draper, UT |
| Affected scope | 59,418 units |
| Distribution | Nationwide to MN, IL, NJ and MI, further distributed nationwide. No foreign/VA/govt/military. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1618-2016) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.. Recalled by Zarbee's Naturals Inc.. Units affected: 59,418 units.
Why was this product recalled? ▼
Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable visual appearance standards for the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on July 13, 2016. Severity: Low. Recall number: F-1618-2016.
Where was the recalled product distributed? ▼
Distribution: Nationwide to MN, IL, NJ and MI, further distributed nationwide. No foreign/VA/govt/military..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1618-2016) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 13, 2016. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.