Baby Vitamin D Dietary supplement — Class III food recall F-1618-2016
Terminated recall by Zarbee's Naturals Inc., reported 2016-07-13, distributed nationwide. Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable visu
| Recall number | F-1618-2016 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zarbee's Naturals Inc., Draper, UT, United States |
| Recall initiated | 2015-09-21 |
| Classified | 2016-07-06 |
| Reported by FDA | 2016-07-13 |
| Terminated | 2017-02-17 |
| Distributed | Nationwide (US) |
| Quantity | 59,418 units |
| Lot numbers | 15042013283, 15049013283, 15100013283, 15113013283, 15118013283, 15119013283, 1517301283, 1517401283 |
| Expiration dates | 2016-05, 2016-07, 2016-09 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1618-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.