Food Recall Check
Class II · Moderate risk Ongoing Initiated Jun 18, 2026 (4 months ago)

Vista MAX Dietary Supplement recall

Recalled by Provision Health Corp. dba PH Labs · San Diego, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Dietary supplement product Vista MAX contains undeclared Yellow#5.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

FDA's distribution note: Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away.

Recalling firm
Provision Health Corp. dba PH Labs
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 18, 2026
In FDA report of
Jul 8, 2026
FDA recall number
H-1135-2026 · event 99294
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Ongoing Labeling

Ocular Plus with Lutein

Reason Dietary supplement product Ocular Plus contains undeclared Yellow#5.

Provision Health Corp. dba PH Labs H-1134-2026

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