Vista MAX Dietary Supplement Recall for Undeclared Yellow #5
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Provision Health Corp. dba PH Labs is recalling 6,967 units of Vista MAX dietary supplements because the product contains undeclared Yellow #5.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 6, 2026 and geographically references California. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Dietary Supplement.
What Happened Provision Health Corp. dba PH Labs initiated a voluntary recall of Vista MAX dietary supplement after it was determined the product contains undeclared Yellow #5.
Which Products Are Affected Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201. UPC: PHF-C023. Affected lots: 509011; 506013; 409012. Expiration dates: 09/27; 06/27; 09/26. A total of 6,967 units across all lots were distributed to two local retail stores in California.
What You Should Do Consumers who have purchased the affected product should stop using it and contact the recalling firm regarding return or refund procedures.
Why This Matters Undeclared Yellow #5 in the dietary supplement may cause allergic reactions in sensitive individuals.
Source FDA recall number H-1135-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (855 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 6, 2026.
Frequently Asked Questions
Common questions about this FDA recall.