Johnson & Johnson
FDA Regulatory Profile
Johnson & Johnson appears in FDA public data with 4 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0244-2018, Class II) was initiated on Dec 7, 2017. Its most recent 510(k) clearance was granted on Oct 1, 2014.
Summary
- Total Recalls
- 4
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| D-0244-2018 | Class II | Neutrogena deep clean purifying whipped foam cleanser, (Salicylic Acid 0.5%), aerosolized product in | Dec 7, 2017 |
| D-0243-2018 | Class II | Neutrogena Acne Proofing whipped foam cleanser, (Salicylic Acid 2%), aerosolized product in a can, N | Dec 7, 2017 |
| D-0245-2018 | Class II | Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean Purifying Whipped Foam Cleanser | Dec 7, 2017 |
| D-098-2013 | Class III | Clean & Clear advantage, 3-in-1 foaming wash 8 FL. OZ. (240 mL) bottle, OTC, Distributed in the US | Dec 4, 2012 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K142460 | EXPEDIUM Spine System/Synapse System | Oct 1, 2014 |
| K113273 | SPOTLIGHT ACCESS SYSTEM | Jan 27, 2012 |
| K112913 | SPOTLIGHT ACCESS SYSTEM | Dec 16, 2011 |
| K113348 | COUGAR SYSTEM | Dec 13, 2011 |
| K110551 | EXPEDIUM SPINE SYSTEM | Oct 26, 2011 |
| K110694 | CONCORDE BULLET SPINAL SYSTEM | Oct 11, 2011 |
| K111571 | VIPER SYSTEMS | Jul 6, 2011 |
| K110454 | COUGAR LS LATERAL CAGE SYSTEM | May 13, 2011 |
| K103743 | CONCORDE CURVE SYSTEM | Mar 17, 2011 |
| K103488 | CONCORDE BULLET CAGE SYSTEM | Mar 2, 2011 |
| K103490 | EXPEDIUM SPINE SYSTEM, MOSS MIAMI SPINE SYSTEM | Feb 17, 2011 |
| K063577 | FEMORAL INTRAFIX SCREW AND SHEATH | Jan 25, 2007 |
| K060914 | TRIDENT ANCHOR | Jun 9, 2006 |
| K060618 | CIDEX ACTIVATED DIALDEHYDE SOLUTION | Apr 12, 2006 |