F-0352-2022 Class II Terminated

Recalled by Golden Lab LLC — Jacksonville, FL

FDA food recall F-0352-2022 was initiated by Golden Lab LLC on Nov 30, 2021 and is designated Class II. Reason for recall: Undeclared fish allergen The recall status is terminated (terminated Mar 15, 2022). Affected quantity: 13,079 units.

Recall Details

Product Type
Food
Report Date
Dec 29, 2021
Initiation Date
Nov 30, 2021
Termination Date
Mar 15, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
13,079 units

Product Description

DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/Dietary Supplement

Reason for Recall

Undeclared fish allergen

Distribution Pattern

Domestic distribution only.

Code Information

Lots: D93210669 and E11290344

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0352-2022
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 8, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for F-0352-2022. Report a data issue: hello@regdatalab.com.