PlainRecalls
ModerateClass IITerminated

FDA Drug recall · Reported February 7, 2018

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

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

Recall #
D-0243-2018
Affected scope
67,260 units
Initiated
December 7, 2017
Verify with FDA Drug →
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Johnson & Johnson recalled Neutrogena Acne Proofing whipped foam cleanser, (Salicylic Acid 2%), aerosolized product … - a moderate-severity action.

Neutrogena Acne Proofing whipped foam cleanser, (Salicylic Acid 2%), aerosolized product … was recalled by Johnson & Johnson in February 7, 2018. Reason: Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container …. Check the official notice for the remedy. Verify recall #D-0243-2018 with the FDA Drug before acting.

The recall

Johnson & Johnson issued this moderate-severity FDA Drug recall-Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container ….

Moderate
severity level
67K units
affected scope
Class II
classification
February 7, 2018
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0243-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,472 drugs & medications recalls on record

05001,0001,5002,000 2006201220152018202120242026 448
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

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

Reason for recall

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

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number D-0243-2018
Date reported February 7, 2018
Date initiated December 7, 2017
Recalling firm Johnson & Johnson
Firm location Skillman, NJ
Affected scope 67,260 units
Distribution Product was distributed nationwide

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

67,260 units units affected - limited or regional distribution scale.

Regional (<10K units) -
Multi-state (10K – 100K units) ✓ This recall
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-0243-2018) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
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. Recalled by Johnson & Johnson. Units affected: 67,260 units.
Why was this product recalled?
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 7, 2018. Severity: Moderate. Recall number: D-0243-2018.
Where was the recalled product distributed?
Distribution: Product was distributed nationwide.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

Compare this recall with Kian Pee Wan Capsules, 30-count bottles → · All Drugs & Medications recalls

This recall: FDA Drug, reported February 7, 2018. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026