Neutrogena Ultra Sheer Sunscreen Recalled for cGMP Deviations
Johnson & Johnson Consumer, Inc. is voluntarily recalling Neutrogena Ultra Sheer body mist sunscreen SPF 30 due to current good manufacturing practice (cGMP) deviations. The recall affects approximately 1.6 million cans distributed nationwide.
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: This is a voluntary, firm-initiated FDA Class II recall for cGMP deviations with no reported illnesses or injuries. The source text provides no evidence of actual harm, making this a precautionary manufacturing compliance recall meeting the "Moderate" criterion.
Plain-English summary
Johnson & Johnson Consumer, Inc. is recalling Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 (5.0 oz aerosol cans, UPC 0 86800 10038 6) distributed nationwide in the United States.
The recall was initiated by the firm due to cGMP (current good manufacturing practice) deviations. This is a voluntary recall initiated by the manufacturer. Approximately 1,611,180 cans are affected, with all lots within their expiration date included in the recall.
No specific adverse events or injuries are detailed in the source information. Consumers should contact Johnson & Johnson Consumer, Inc. with any questions or concerns about this product.
The recalled product
- Product
- Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30, Avobenzone (3%), Homosalate (8%), Octisalate (5%), Octocrylene (8%), Net Wt. 5.0 OZ (141 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NY 08858 UPC 0 86800 10038 6
- Manufacturer
- Johnson & Johnson Consumer, Inc.
- Category
- Drug — Sunscreen / Topical
- Hazard
- Affected units
- 1,611,180
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 (1)
- All lots within expiry
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 20 recalled by Johnson & Johnson Consumer, Inc. 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 20 products in this recall →Related recalls
Same manufacturer · Johnson & Johnson Consumer, Inc.
See all →- ModerateNeutrogena Beach Defense Sunscreen Spray Recalled for cGMP Deviations
FDA (Drugs) · 2021-10-06
- ModerateNeutrogena Ultra Sheer SPF 30 Body Mist Sunscreen Recall
FDA (Drugs) · 2021-10-06
- SevereNeutrogena Beach Defense Sunscreen Spray Recalled for Benzene Contamination
FDA (Drugs) · 2021-10-06
- ModerateNeutrogena Ultra Sheer Sunscreen Recalled for cGMP Deviations
FDA (Drugs) · 2021-10-06
- ModerateNeutrogena Beach Defense Sunscreen Spray Class II Drug Recall
FDA (Drugs) · 2021-10-06
Same hazard · cgmp deviation
See all →- HighBaxter Recalls Clindamycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- SevereBaxter Recalls Clindamycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- SevereBaxter Recalls Daptomycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- HighBaxter Recalls Clindamycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- ModerateBaxter Recalls Clindamycin Phosphate Injection Due to CGMP Deviations
FDA (Drugs) · 2026-09-09