Recall archive / FDA food enforcement
DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/Dietary Supplement — FDA record F-0352-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Nov 30, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/Dietary Supplement
- Reason
- Undeclared fish allergen
- Classification
- Class II
- Recalling firm
- Golden Lab LLC
- Quantity
- 13,079 units
- Agency-reported status
- Terminated
- Source record identifier
- F-0352-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lots: D93210669 and E11290344 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Domestic distribution only.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Dec 29, 2021
- Recall initiation date
- Nov 30, 2021
- Center classification date
- Dec 23, 2021
- Termination date
- Mar 15, 2022
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.