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RECALL RECORD — CLASS IIRecall closedF-0352-2022/FDA enforcement
Golden Lab LLC·Dietary Supplements·Nov 30, 2021

Doctorx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/dietary…

What you need to know

Class II

  • What happened

    Undeclared fish allergen

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Fish-derived ingredients were omitted from the label, creating a risk for fish-allergic consumers.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDADistribution not listedMore supplements

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Product identification

Source: FDA FOOD

Brand nameGolden Lab LLC
Recalling firmGolden Lab LLCJacksonville, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lots: D93210669 and E11290344
Distribution area

Domestic distribution only.

United States

Quantity affected13, 079 units
Recall initiationFDA report date: December 29, 2021
FDA recall numberF-0352-2022

Beyond the headline

The recall, in context

Golden Lab LLC initiated this supplements recall on November 30, 2021. The FDA enforcement report states: Undeclared fish allergen. The FDA report lists distribution as: Domestic distribution only.

The FDA enforcement report describes the reason as: Undeclared fish allergen

Doctorx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/dietary… was made or distributed by Golden Lab LLC in Jacksonville, FL, United States. This page reflects FDA report F-0352-2022, dated December 29, 2021.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared fish

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a fish allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Doctorx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/dietary… recall?

Golden Lab LLC recalled Doctorx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/dietary… in an FDA Class II enforcement action reported as F-0352-2022. Undeclared fish allergen

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Do not eat the product if you have a fish allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Golden Lab LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0352-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.