Vista MAX Supplement Recalled for Undeclared Yellow #5 Dye

Provision Health Corp., doing business as PH Labs, has voluntarily recalled 6,967 units of Vista MAX dietary supplement after discovering the product contains undeclared Yellow #5, a color additive not listed on the product label. The recall, numbered H-1135-2026, has been classified as Class II by the FDA, meaning use of the product may cause temporary or medically reversible health effects.

What Products Are Being Recalled?

The recall covers Vista MAX Dietary Supplement, sold in bottles of 90 capsules with a serving size of 4 capsules. The product carries UPC PHF-C023 and was distributed by Vision of Health, based in Bell, CA 90201. Three lots are affected: 509011, 506013, and 409012, with expiration dates of 09/27, 06/27, and 09/26 respectively.

Why Was This Recall Issued?

The recall was initiated after it was determined that Vista MAX contains Yellow #5, a synthetic color additive, which was not disclosed on the product’s ingredient label. Failure to declare this additive means consumers with sensitivities or allergies to Yellow #5 were not properly informed before use. Undeclared color additives can trigger allergic-type reactions in sensitive individuals, including hives, itching, or respiratory symptoms, and consumers relying on accurate labeling to avoid the ingredient were denied that ability.

Who Is Affected?

According to the FDA enforcement report, the affected product was distributed to two local direct accounts, both of which are local retail stores selling vitamins and health products. The recall is limited in scope, and the firm initiated the action voluntarily after notifying consignees by letter. No press release has been issued for this recall, and it remains classified as ongoing as of the FDA’s Center Classification Date of July 1, 2026.

What Should You Do?

1. Stop use immediately if you purchased Vista MAX with any of the affected lot numbers, especially if you have a known sensitivity or allergy to Yellow #5.

• Check the lot number and expiration date printed on your bottle against 509011 (exp 09/27), 506013 (exp 06/27), or 409012 (exp 09/26).
• If you purchased the product from one of the two affected retail stores, contact the store directly for return or refund information.
• Consumers experiencing an allergic reaction after using Vista MAX should consult a healthcare provider.
• For further information, contact the recalling firm, Provision Health Corp. dba PH Labs, at 9760 Via De La Amistad, San Diego, CA 92154-7210, United States.

Official Statement

The FDA enforcement report lists the recall as ‘Voluntary: Firm Initiated’ with an initial notification method of ‘Letter’ sent to consignees. The recall was initiated on June 18, 2026, and remains ongoing, with no termination date recorded at this time. No formal press release has been issued for this recall, and the report notes there is no update history available for this product beyond its original listing.