PlainRecalls
ModerateClass IIOngoing

FDA Food recall · Reported July 8, 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

Dietary supplement product Ocular Plus contains undeclared Yellow#5.

Recall #
H-1134-2026
Affected scope
6,967 units across all lots
Initiated
June 18, 2026
Verify with FDA Food →
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Provision Health Corp. dba Ph Labs recalled Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. S… - a moderate-severity action.

Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. S… was recalled by Provision Health Corp. dba Ph Labs in July 8, 2026. Reason: Dietary supplement product Ocular Plus contains undeclared Yellow#5.. Check the official notice for the remedy. Verify recall #H-1134-2026 with the FDA Food before acting.

The recall

Provision Health Corp. dba Ph Labs issued this moderate-severity FDA Food recall-Dietary supplement product Ocular Plus contains undeclared Yellow#5..

Moderate
severity level
7K units
affected scope
Class II
classification
July 8, 2026
reported

Sourced from official FDA Food enforcement records. Verify recall #H-1134-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #H-1134-2026) was formally reported on July 8, 2026, with the manufacturer initiating the action on June 18, 2026. It is classified under Moderate severity (Class II), with a current status of Ongoing. Provision Health Corp. dba Ph Labs is listed as the recalling firm, operating out of San Diego, CA. Federal records list the affected scope as 6,967 units across all lots.

The documented reason for this recall is: Dietary supplement product Ocular Plus contains undeclared Yellow#5. Distribution data in the federal record shows the product reached: Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Dietary Supplements recalls over time

Where this recall sits in its category - 2,012 dietary supplements recalls on record

0100200300400 20072010201320162019202220252026 19
Severity1902064468High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Moderate

Affected scope

6,967 units across all lots

Related Recalls

6

6 from same agency

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

Reason for recall

Dietary supplement product Ocular Plus contains undeclared Yellow#5.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Ongoing
Recall number H-1134-2026
Date reported July 8, 2026
Date initiated June 18, 2026
Recalling firm Provision Health Corp. dba Ph Labs
Firm location San Diego, CA
Affected scope 6,967 units across all lots
Distribution Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

6,967 units across all lots units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units) -
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (H-1134-2026) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product 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. Recalled by Provision Health Corp. dba Ph Labs. Units affected: 6,967 units across all lots.
Why was this product recalled?
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
Which agency issued this recall?
This recall was issued by the FDA Food on July 8, 2026. Severity: Moderate. Recall number: H-1134-2026.
Where was the recalled product distributed?
Distribution: Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products..
How do I check if my product is affected by a recall?
Check the product description and recall number (H-1134-2026) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.

Nearby Recalls in This Category

Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.

Showing 5 of 2015 other recalls in this category.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 8, 2026. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.