Recall · openFDA Food Enforcement

Vista MAX: FDA Recall H-1135-2026

Agency action: Jun 18, 2026Record ID: H-1135-2026
View official source ↗

What happened

Original notice title

Vista MAX, recall H-1135-2026

From the archived source record

Dietary supplement product Vista MAX contains undeclared Yellow#5.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Ongoing
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
Jul 8, 2026
Source checked
Jul 16, 2026
Record revision
68e8494e267d

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023
Company
Provision Health Corp. dba PH Labs
Lot / identifier
Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
Market / distribution
Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.