D-0833-2021 Class II Ongoing
FDA drug recall D-0833-2021 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) 1,265,724 b) 1,052,544cans.
Recall details
- Product Type
- Drugs
- Report Date
- Oct 6, 2021
- Initiation Date
- Jul 14, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- a) 1,265,724 b) 1,052,544cans
Product description
Neutrogena Beach Defense water + sun protection sunscreen spray BROAD SPECTRUM SPF 30, Avobenzone (3%), Homosalate (8%), Octisalate (5%), Octocrylene (8%), a) NET WT. 6.5 OZ (184 g) (UPC 0 86800 87273 3) and b) NET WT. 8.5 oz (240 g) (UPC 0 86800 10032 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-0833-2021
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026