Why it was recalled
Undeclared fish allergen
Product description
DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/Dietary Supplement
Lot numbers, UPCs & expiration codes
Lots: D93210669 and E11290344
Where it was sold
Domestic distribution only.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0352-2022
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Nov 30, 2021
- FDA report date
- Dec 29, 2021
- Quantity
- 13,079 units
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Golden Lab LLC
Original FDA data
Every field from FDA enforcement report F-0352-2022, exactly as published.
Show all FDA fields
- City
- Jacksonville
- State
- FL
- Status
- Terminated
- Country
- United States
- Event ID
- 89068
- Address
- 2375 Saint Johns Bluff Rd S Ste 310
- Code information
- Lots: D93210669 and E11290344
- Postal code
- 32246-2335
- Report date
- Dec 29, 2021
- Product type
- Food
- Recall number
- F-0352-2022
- Classification
- Class II
- Recalling firm
- Golden Lab LLC
- Product quantity
- 13,079 units
- Termination date
- Mar 15, 2022
- Reason for recall
- Undeclared fish allergen
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/Dietary Supplement
- Distribution pattern
- Domestic distribution only.
- Recall initiation date
- Nov 30, 2021
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Dec 23, 2021