CLASS II Food recall · Reported 29 Dec 2021 · FDA Enforcement Report
DoctoRx's Optimal Formula, Dry Eye Formula recalled by Golden Lab
Golden Lab is recalling DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel/Dietary Supplement. The recall was initiated on 30 Nov 2021 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0352-2022
- FDA event ID
- 89068
- Recalling firm
- Golden Lab, Jacksonville, FL
- Brand
- DoctoRx's Optimal
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 30 Nov 2021
- FDA classified
- 23 Dec 2021
- Reported
- 29 Dec 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Fish & Shellfish
- Product category
- Dietary Supplements
Timeline
| 30 Nov 2021 | Recall initiated by company | |
| 23 Dec 2021 | Classified by FDA | +23 days |
| 29 Dec 2021 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared fish allergen
Product as listed by the FDA
DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/Dietary Supplement
Where it was distributed
Domestic distribution only.
Questions about this recall
Why was it recalled?
Undeclared fish allergen
Which lots are affected?
Lots: D93210669 and E11290344
Where was it sold?
Domestic distribution only.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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