FDAClass II · Food · Recall H-1134-2026 · Recalled July 8, 2026

Ocular Plus with Lutein recall — Provision Health Corp. dba PH Labs

Agency report date: July 8, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Ocular Plus with Lutein
Company / brand: Provision Health dba PH Labs
Lot / serial / date codes: Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
Distribution: Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Dietary supplement product Ocular Plus contains undeclared Yellow#5.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Ocular Plus with Lutein

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1134-2026
Brand: Provision Health dba PH Labs
Classification: Class II
Units affected: 6,967 units across all lots
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Ocular Plus with Lutein

Companies & origin

Recalling firm location: San Diego, CA, United States
Firm address: 9760 Via De La Amistad, N/A, 92154-7210

Identifying details (verbatim from the notice)

Product codes / lots: Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26
Distribution: Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
Firm notified the public via: Letter
FDA event ID: 99294
Recall initiated: June 18, 2026
FDA classified: July 1, 2026
FDA report date: July 8, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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