Fruit & Vegetable Supplement

Balance Of Nature Whole Produce Fruits

48 adverse event reports submitted to the FDA · 2023–2025 · Data current as of June 3, 2026

These are reports submitted to the FDA. A report does not mean the product caused the effect. Counts reflect reporting activity, not how common an effect is.

Most Reported Reactions

Top 10 reactions from 48 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Drug interaction
5
Blood glucose increased
5
Choking
4
Myocardial infarction
4
Pain
4
Diarrhoea
4
Malaise
4
Dyspnoea
4
Intestinal obstruction
3
Foreign body in throat
2

Reported Outcomes

Outcome categories as recorded in FDA reports. One report may include multiple outcomes.

OutcomeReports
Other Serious or Important Medical Event 33
Hospitalization 28
Visited Emergency Room 15
Life Threatening 3
Visited a Health Care Provider 3
Allergic Reaction 1

Who Reported

Reporter demographics where available. Many reports do not include age or gender data.

Age

Under 18
0
18–34
0
35–49
0
50–64
5
65–79
13
80+
10
Unknown
20

28 reports had age data; 20 unknown.

Gender

Female
20
Male
25
Unknown/Not Reported
3

Reports by Year

Annual report counts from 2023–2025. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'23
'24
'25

Hover bars for exact counts.

Context about this data: Reports concentrated in 2025 (52% of total, spanning 2023–2025), suggesting a reporting event during that period rather than evenly distributed consumer use.

Data Source

This page presents data from the FDA's CFSAN Adverse Event Reporting System (CAERS) via the openFDA API. Reports are voluntary and unverified. The FDA has not concluded that this product caused any reported event.

View openFDA CAERS data ↗  ·  About our methodology  ·  How to read this data