On June 18 2026 the U.S. Food & Drug Administration entered an official recall for the dietary supplement Vista MAX, manufactured by Provision Health Corp. dba PH Labs in San Diego, California. The action was prompted by the detection of the synthetic dye Yellow #5 in bottles that did not list the ingredient on their label.1
Why the Recall Was Initiated
The FDA record states that the product contained undeclared Yellow #5, a color additive that had not been disclosed on the product’s ingredient panel. Because the supplement did not communicate the presence of this dye, it could contravene labeling rules that require full ingredient disclosure for dietary supplements.1
Product Composition and Distribution
- Product name: Vista MAX
- Form: 90 capsules
- Serving size: 4 capsules
- Distributor: Vision of Health, Bell, CA 90201
- UPC: PHF-C023
- Recall status: Class II, ongoing
- Recall initiation date: 2026‑06‑18
- Lot numbers affected: 509011, 506013, 409012
- Expiration dates: 09/27, 06/27, 09/26
The product was distributed to two local direct accounts, each at a retail store that sells a variety of vitamins and health products. No other retail locations are named in the FDA record.1
Regulatory Context
Under FDA enforcement guidelines, recalls are categorized by severity. A Class II recall is applied when a product might cause temporary health problems or a significant health risk if not withdrawn. The recall of Vista MAX is classified as Class II, indicating the FDA considers the undeclared Yellow #5 a potential health concern that necessitates removal from the market.1
What This Means for Consumers
Consumers who purchase products labeled as Vista MAX should verify whether their purchase is among the recalled lots by checking the sequence of numbers on the bottle. The FDA record lists the affected lot numbers but does not provide explicit instructions for product return or refund. Current recall status is ongoing, so the product remains on the market until corrective action is completed.1
Bottom Line
Evidence from the FDA recall record confirms that Provision Health Corp.’s Vista MAX capsules contain an undeclared synthetic dye, Yellow #5, which is not listed on the label. The product has been classified as a Class II recall and distribution continues only in a limited local context. No further data are available from the record regarding the extent of potential health impacts or steps taken by the manufacturer to remove the dye from future batches.