Neptune Resources, LLC: Drug Recall

Recall #D-0335-2024 · 01/12/2024

Class I: Dangerous

Recall Details

Recall Number
D-0335-2024
Classification
Class I
Product Type
Drug
Recalling Firm
Neptune Resources, LLC
Status
Ongoing
Date Initiated
01/12/2024
Location
Kansas City, MO, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
4,932 boxes

Reason for Recall

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

Product Description

Neptune's Fix, Tianeptine Tablets Extended Relief, Twenty Tablets per Box, Wide Awake, 3000 mg (150 mg Per Tablet), Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

Distribution Pattern

Nationwide in the USA

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.