Parker Laboratories, Inc.: Drug Recall

Recall #D-1093-2023 · 08/02/2023

Class II: Risk

Recall Details

Recall Number
D-1093-2023
Classification
Class II
Product Type
Drug
Recalling Firm
Parker Laboratories, Inc.
Status
Terminated
Date Initiated
08/02/2023
Location
Fairfield, NJ, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
50

Reason for Recall

CGMP Deviations

Product Description

Helix CBD Clinical Cream (Menthol 7.4%), packaged in a)3 gm pouches (NDC30775-054-01), b)2 fl. oz. tubes (NDC 30775-054-02), and c) 4 fl. oz. tubes (NDC 30775-054-04), Parker Laboratories, Inc. 286 Eldridge Road, Fairfield, NJ 07004

Distribution Pattern

Nationwide within the United States, Singapore, Korea and Hong Kong

Other Recalls by Parker Laboratories, Inc.

View all recalls by Parker Laboratories, Inc. →

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.