D-0244-2018 Class II Terminated

Recalled by Johnson & Johnson — Skillman, NJ

FDA drug recall D-0244-2018 was initiated by Johnson & Johnson on December 7, 2017 and is designated Class II. Reason for recall: Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area. The recall status is terminated (terminated September 9, 2019).

Recall Details

Product Type
Drugs
Report Date
February 7, 2018
Initiation Date
December 7, 2017
Termination Date
September 9, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity

Product Description

Neutrogena deep clean purifying whipped foam cleanser, (Salicylic Acid 0.5%), aerosolized product in a can, NET WT. 5 OZ. (141 g) Distributed By: Johnson & Johnson Consumer Inc. Skillman, NJ 08558. UPC: 0 70501 10053 0

Reason for Recall

Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.

Distribution Pattern

Product was distributed nationwide

Code Information

Lot #:15917F54, 16017F54, Exp. 05/2019; 15817F69,15917F69, Exp. 04/2019; 20017F55, 20117F55, Exp. 06/2019.