Provision Health Corp. dba PH Labs Recall: Dietary supplement product Vista MAX contains undeclared Yellow#5.

🇺🇸 United States

1. June 18, 2026 - Recall initiated
2. July 8, 2026 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-1135-2026

Event ID

99294

Status

Ongoing

Classification

Class II

Company

Provision Health Corp. dba PH Labs

Product description

Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023

Quantity

6,967 units across all lots

Reason

Dietary supplement product Vista MAX contains undeclared Yellow#5.

Recall initiation date

June 18, 2026

Report date

July 8, 2026

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.

UPC, lot, and code information

Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 99294 with 1 other product entry in Public Health Trace.

Responsible company: Provision Health Corp. dba PH Labs

Other recalls from Provision Health Corp. dba PH Labs

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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