Recall events
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Event 72250
Event summary
Timeline bucket September 21, 2015
Product types Food
Classifications Class III
Statuses Terminated
Recalling firm wording Zarbee's Naturals Inc.
Dossier provenance
Source snapshots represented here
openFDA Food Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
2 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
food · product 1 of 2
Baby Omega 3 Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
F-1617-2016
Recall number F-1617-2016
Initiated September 21, 2015
Classification Class III
Status Terminated
Quantity 41,565 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable visual appearance standards for the product.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
Code information Lot# 15043013284, expiry 05/2016 Lot# 15100013284, expiry 07/2016 Lot# 15114013284, expiry 07/2016 Lot# 1516901284, expiry 09/2016 Lot# 1517001284, expiry 09/2016
Distribution pattern Nationwide to MN, IL, NJ and MI, further distributed nationwide. No foreign/VA/govt/military.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[16507]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 2
Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
F-1618-2016
Recall number F-1618-2016
Initiated September 21, 2015
Classification Class III
Status Terminated
Quantity 59,418 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Some units of each lot may contain contaminants (elevated aerobic plate count) and do not meet acceptable visual appearance standards for the product.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
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.
Code information Lot# 15042013283, expiry 05/2016 Lot# 15049013283, expiry 05/2016 Lot# 15100013283, expiry 07/2016 Lot# 15113013283, expiry 07/2016 Lot# 15118013283, expiry 07/2016 Lot# 15119013283, expiry 07/2016 Lot# 1517301283, expiry 07/2016 Lot# 1517401283, expiry 09/2016
Distribution pattern Nationwide to MN, IL, NJ and MI, further distributed nationwide. No foreign/VA/govt/military.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[16535]
FDA event record
· Exact recall-number query on openFDA
