CLASS II ONGOING Food recall · Reported 8 Jul 2026 · FDA Enforcement Report
Vista MAX; Dietary Supplement Serving Size recalled by Provision Health
Provision Health is recalling Vista MAX; Dietary Supplement Serving Size. The recall was initiated on 18 Jun 2026 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-1135-2026
- FDA event ID
- 99294
- Recalling firm
- Provision Health, San Diego, CA
- Brand
- Vista MAX
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 18 Jun 2026
- FDA classified
- 1 Jul 2026
- Reported
- 8 Jul 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Allergens
- Product category
- Dietary Supplements
Timeline
| 18 Jun 2026 | Recall initiated by company | |
| 1 Jul 2026 | Classified by FDA | +13 days |
| 8 Jul 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Dietary supplement product Vista MAX contains undeclared Yellow#5.
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023
Where it was distributed
Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
Questions about this recall
Why was it recalled?
Dietary supplement product Vista MAX contains undeclared Yellow#5.
Which lots are affected?
Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
Where was it sold?
Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 99294| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Ocular Plus with Lutein, Zeaxanthin, and Omega recalledOcular Plus | Provision Health | Undeclared Allergens | CA |
More recalls from Provision Health
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Ocular Plus with Lutein, Zeaxanthin, and Omega recalledOcular Plus | Provision Health | Undeclared Allergens | CA |
Other Dietary Supplements recalls
All 733| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
| Food | CLASS I | Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR | ZMB Enterprises | Hidden Drug Ingredients | CA |
| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Imu-Tek Colostrum recalled by Imu-Tek Animal HealthImu-Tek Colostrum-5 | Imu-Tek Animal Health, Incorporated | Foreign Material | 30 states |