Food recall: Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size: 4 Capsules…
Class II FDA enforcement event 99294. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Provision Health Corp. dba PH Labs started this food recall on 18 Jun 2026. The firm address in the FDA record is in San Diego, CA. FDA put the recall in Class II. FDA event 99294 has 2 product records. The first FDA enforcement report date is 8 Jul 2026. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
Recalling firm
Provision Health Corp. dba PH Labs, San Diego, CA.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
2 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| H-1134-2026 | 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 | 6,967 units across all lots | Class II | Ongoing | 8 Jul 2026 |
| H-1135-2026 | Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023 | 6,967 units across all lots | Class II | Ongoing | 8 Jul 2026 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2026
- 304
- Share of these events in Class II
- 53%
- Product records in this event
- 2
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report H-1134-2026The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 99294. https://recallregister.com/fda/ii/99294/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
- What quantity of product is in FDA event 99294?
- The event has 2 product records. The first record gives this quantity:
6,967 units across all lots
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2026 have the same class?
- 53% of the 304 food events that started in 2026 are in Class II.