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FDAClass II · Food · Recalled July 8, 2026
Vista MAX recall — Provision Health Corp. dba PH Labs
Hazard: Dietary supplement product Vista MAX contains undeclared Yellow#5.
Class II: may cause temporary or medically reversible health consequences.
View the official FDA enforcement record (openFDA) ↗
- Official recall ID
- H-1135-2026
- Brand
- Provision Health dba PH Labs
- Classification
- Class II
- Units affected
- 6,967 units across all lots
- Recall status
- Ongoing
- Initiated
- Voluntary: Firm initiated
Description
Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023
Affected products
Companies & origin
- Recalling firm location
- San Diego, CA, United States
- Firm address
- 9760 Via De La Amistad, N/A, 92154-7210
Identifying details (verbatim from the notice)
- Product codes / lots
- Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
- Distribution
- Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
- Firm notified the public via
- Letter
- FDA event ID
- 99294
- Recall initiated
- June 18, 2026
- FDA classified
- July 1, 2026
- FDA report date
- July 8, 2026
Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim;
the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.
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