H-1135-2026
Provision Health Corp. dba PH Labs
Data retrieved 2026-10-27T22:06:49.008Z
Site-assigned category (for this product recall): Allergen & mislabeling
Independent website; not affiliated with or endorsed by FDA. Recall information is attributed to the linked FDA record. Categories are assigned by this website using keyword rules; they are not FDA classifications or independent legal findings and may be incomplete or incorrect. A category summarizes the stated reason for the identified product recall, not a finding about the firm generally or its other products. FDA’s original reason text appears below.
Official openFDA record · FDA recalls and safety alerts
Fields as reported by FDA
Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.
- recall_number
- H-1135-2026
- event_id
- 99294
- recalling_firm
- Provision Health Corp. dba PH Labs
- city
- San Diego
- state
- CA
- country
- United States
- product_description
- Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023
- reason_for_recall
- Dietary supplement product Vista MAX contains undeclared Yellow#5.
- classification
- Class II
- FDA-reported status (not current status)
- Ongoing
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated. - voluntary_mandated
- Voluntary: Firm initiated
- distribution_pattern
- Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
- product_quantity
- 6,967 units across all lots
- code_info
- Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
- recall_initiation_date
- 2026-06-18
- report_date
- 2026-07-08
- termination_date
- Not reported