Vista MAX Dietary Supplement
Reason Dietary supplement product Vista MAX contains undeclared Yellow#5.
Ocular Plus with Lutein recall
Recalled by Provision Health Corp. dba PH Labs · San Diego, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size: 4 Capsules; Distributed by: L.A. Farmacia Natural, Burbank, CA 91504 UPC: PHF-C023
Quantity: 6,967 units across all lots
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
Where it was sold
FDA's distribution note: Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away.
- Recalling firm
- Provision Health Corp. dba PH Labs
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 18, 2026
- In FDA report of
- Jul 8, 2026
- FDA recall number
- H-1134-2026 · event 99294
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.