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Use caution Food recall · FDA · Published June 18, 2026

PH Labs Recalls Vista MAX Due to Undeclared Yellow #5

Provision Health Corp. recalls Vista MAX dietary supplement (90 capsules) due to undeclared Yellow #5. Check your lot numbers and expiration dates.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-1135-2026FoodPH Labs ›
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Recalling firmProvision Health Corp. dba PH Labs9760 Via De La Amistad · San Diego, CA 92154-7210
✎ GovInfoNow plain-language explainer

Provision Health Corp., doing business as PH Labs, is recalling Vista MAX, a dietary supplement sold in 90-capsule bottles. The product contains undeclared Yellow #5, an artificial food dye that may cause allergic reactions in sensitive individuals. The recall covers 6,967 units distributed to two local retail accounts in the Bell, CA area. Read more at govinfonow.com/recall/6182-ph-labs-recalls-vista-max-due-to-undeclared-yellow-5.

Source Summary by GovInfoNow · govinfonow.com/recall/6182-ph-labs-recalls-vista-max-due-to-undeclared-yellow-5 · Updated October 9, 2026 · Official notice: FDA #H-1135-2026

Cite this page

“PH Labs Recalls Vista MAX Due to Undeclared Yellow #5.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6182-ph-labs-recalls-vista-max-due-to-undeclared-yellow-5. Based on FDA recall #H-1135-2026.

The FDA announced on June 18, 2026, that Provision Health Corp. dba PH Labs is recalling Vista MAX dietary supplement due to undeclared Yellow #5. The firm initiated this voluntary Class II recall affecting 6,967 units.

How to tell if you have it

  • Brand: PH Labs
  • Product: Vista MAX Dietary Supplement, 90 Capsules
  • UPC: PHF-C023
  • Lots: 509011, 506013, 409012
  • Expiration dates: 09/27, 06/27, 09/26
  • Distributed by Vision of Health, Bell, CA 90201

The hazard

The Vista MAX dietary supplement contains undeclared Yellow #5, according to the FDA. The agency classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include King Calypso Tropic Tango Lemonade Recall (2026-04-23) and Galaxy RG Corp Jumbo Neapolitan Recall (2026-04-03). Another similar recall was the Galaxy RG Corp Guava Rolls Recall on 2026-04-03.

How to tell if you have this one

Check your bottle for the brand name 'Vista MAX' and the UPC code PHF-C023. Verify the lot numbers are one of the following: 509011, 506013, or 409012. Confirm the expiration date is 09/27, 06/27, or 09/26.

  • Brand
    PH Labs
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
Recall numberProduct, codes & lots
H-1134-2026Ocular 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; Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
H-1135-2026Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023; Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not take the Vista MAX capsules if you have any of the affected lot numbers or expiration dates.

  2. Check your bottle details

    Verify the UPC (PHF-C023) and lot numbers (509011, 506013, 409012) to confirm if your item is part of this recall.

  3. Contact the distributor

    Reach out to Vision of Health in Bell, CA, for further instructions on returns or refunds.

How this recall unfolded

Recall timeline

FDA published this recall 20 days after the firm started it.

1. Firm started the recall: Jun 18, 202612. FDA classified it Class II: Jul 1, 202623. Published in FDA’s Enforcement Report: Jul 8, 202632026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-1135-2026 (June 18, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA