Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size: 4 Capsules; Distri
Summary
The FDA issued a Class II for Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Ca by Provision Health Corp. dba PH Labs. Reason: Dietary supplement product Ocular Plus contains undeclared Yellow#5..
Details
Source
Food Recall
External ID
H-1134-2026
Action Date
2026-07-08
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
Quantity Affected: 6,967 units across all lots
Reason for Recall
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
Distribution
Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-18
Company
San Diego, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 54 food recalls issued in the same week, part of 101 food-related FDA actions this month.
Provision Health Corp. dba PH Labs has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Provision Health Corp. dba PH Labs) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Provision Health Corp. dba PH Labs have FDA actions?
Provision Health Corp. dba PH Labs has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1134-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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