Food recall

Provision Health Corp. dba PH Labs recall: Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9

Provision Health Corp. dba PH Labs, of San Diego, CA, recalled Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9 and 1 other product. The FDA's reason: “Dietary supplement product Ocular Plus contains undeclared Yellow#5.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on June 18, 2026, and the FDA first listed it in its Enforcement Report of July 8, 2026. The recall is still going on.

How serious

Class II

It could cause temporary or minor harm

Why

Other ingredient not on the label (sulfites, dyes...)

Status

Ongoing

The recall

Company
Provision Health Corp. dba PH Labs (San Diego, CA)
Reason, in FDA's words
“Dietary supplement product Ocular Plus contains undeclared Yellow#5.”
Where it was sold
Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
99294

The 2 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-1134-2026 Class II

    Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size: 4 Capsules; Distributed by: L.A. Farmacia Natural, Burbank, CA 91504 UPC: PHF-C023

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

    Quantity: 6,967 units across all lots

  • H-1135-2026 Class II

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

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

    Quantity: 6,967 units across all lots

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 8, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.