D-0837-2021 Class II Ongoing
FDA drug recall D-0837-2021 was initiated by Johnson & Johnson Consumer, Inc. on Jul 14, 2021 and is designated Class II. Reason for recall: cGMP Deviations The recall status is ongoing. Affected quantity: a) 5oz-1,282,488; b) 8oz-475,476 cans.
Recall details
- Product Type
- Drugs
- Report Date
- Oct 6, 2021
- Initiation Date
- Jul 14, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- a) 5oz-1,282,488; b) 8oz-475,476 cans
Product description
Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 45, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), a) Net Wt. 5 OZ (141 g) (UPC 0 86800 10039 3) and b) Net Wt. 8.0 oz. (226 g) (UPC 0 86800 11134 4) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ, 08858,
Reason for recall
cGMP Deviations
Distribution pattern
Nationwide in US
Code information
All lots within expiry.
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0837-2021
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026