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Stop using now Food recall · FDA · Published November 30, 2021

DoctoRx Recalls Eye Supplements Due to Undeclared Fish Allergen

Golden Lab LLC recalls DoctoRx eye supplements due to undeclared fish allergen. Check your lot numbers D93210669 and E11290344 immediately.

🇺🇸 FDA recall #F-0352-2022FoodDoctoRx ›
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Recalling firmGolden Lab LLC2375 Saint Johns Bluff Rd S Ste 310 · Jacksonville, FL 32246-2335
✎ GovInfoNow plain-language explainer

Golden Lab LLC is recalling specific lots of DoctoRx dietary supplements because they contain an undeclared fish allergen. This poses a risk to individuals with fish allergies who may unknowingly consume the product. The recall covers 13,079 units distributed domestically. Read more at govinfonow.com/recall/13696-doctorx-recalls-eye-supplements-due-to-undeclared-fish-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/13696-doctorx-recalls-eye-supplements-due-to-undeclared-fish-allergen · Updated October 10, 2026 · FDA enforcement record: FDA #F-0352-2022

Cite this page

“DoctoRx Recalls Eye Supplements Due to Undeclared Fish Allergen.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/13696-doctorx-recalls-eye-supplements-due-to-undeclared-fish-allergen. Based on FDA recall #F-0352-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0352-2022%22&limit=1).

The FDA announced on 2021-11-30 that Golden Lab LLC voluntarily recalled DoctoRx's Optimal Formula, Dry Eye Formula, and Ocular Support Softgel dietary supplements due to undeclared fish allergen. Owners should contact the company for a refund. The recall involves 13,079 units distributed domestically.

How to tell if you have it

  • Brand: DoctoRx
  • Products: Optimal Formula Dietary Supplement, Dry Eye Formula, Ocular Support Softgel
  • Size: 60 Softgels
  • Lots: D93210669, E11290344

The hazard

The products contain undeclared fish allergen, posing a risk to individuals with fish allergies. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar dietary supplements include PH Labs Ocular Plus (2026-06-18), Mellish Island Super Skin (2026-07-01), and Vital Nutrients Aller-C (2026-03-27).

How to tell if you have this one

Check your bottle for the lot numbers D93210669 or E11290344. The recalled items are DoctoRx's Optimal Formula, Dry Eye Formula, and Ocular Support Softgel, each containing 60 softgels.

  • Brand
    DoctoRx
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat or use the supplement if it matches the recalled lot numbers.

How this recall unfolded

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Nov 30, 202112. FDA classified it Class II: Dec 23, 202123. Published in FDA’s Enforcement Report: Dec 29, 202134. FDA terminated the recall: Mar 15, 2022420212022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0352-2022 (November 30, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0352-2022 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA