The Recall Desk
ModerateFDA (Drugs)·D-0243-2018·Announced 2018-02-07

Neutrogena Acne Proofing Cleanser Recalled for Container Leakage

Johnson & Johnson is recalling Neutrogena Acne Proofing whipped foam cleanser because the containers may leak propellant and product.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the hazard is a container defect causing leakage without reported injuries or illnesses, fitting the criteria for a moderate severity precautionary recall.

Plain-English summary

Johnson & Johnson is recalling Neutrogena Acne Proofing whipped foam cleanser, an aerosolized product in a can. The recall involves 67,260 units distributed nationwide. The affected product is identified by lot numbers 16217F70, 16317F70, 18317F56, 18417F56, 18517F56, 18617F56, 19517F57, 19617F57, 19717F57, and 19817F57, with an expiration date of 05/2019.

The recall was initiated due to a defective container issue where products showed leakage of propellant and product from the container valve cup area, manifesting as bubbles and foaming. The agency has classified this recall as Class II.

Consumers should check their products for the listed lot numbers and expiration date. If the product is affected, consumers should stop using it and follow instructions from the recalling firm or the FDA regarding disposal or return.

The recalled product

Product
Neutrogena Acne Proofing whipped foam cleanser, (Salicylic Acid 2%), aerosolized product in a can, NET WT. 5 OZ (141 g) , Distributed by Johnson & Johnson Consumer Inc. Skillman, NJ 08558, UPC 0 70501 11131 4
Manufacturer
Johnson & Johnson
Category
Consumer Product — Personal Care
Hazard
Affected units
67,260

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (10)

  • Lot #: 16217F70
  • 16317F70
  • 18317F56
  • 18417F56
  • 18517F56
  • 18617F56
  • 19517F57 19617F57
  • 19717F57
  • 19817F57
  • Exp. 05/2019.

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 3 recalled by Johnson & Johnson under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 3 products in this recall →

Related recalls

Same manufacturer · Johnson & Johnson

See all →

Same hazard · container leakage

See all →