Obagi Nu-derm System Normal-oily Skin Transformation recalls
Obagi Nu-derm System Normal-oily Skin Transformation products have been recalled 1 time, most recently on 12 Nov 2014. The recalling company is usually Obagi Medical Products. The most common reason is packaging defects.
Total recalls1since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 12 Nov 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why obagi nu-derm system normal-oily skin transformation is recalled
Companies
Product types
By year
All obagi nu-derm system normal-oily skin transformation recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Obagi Nu-Derm Clear, AM PM 3, Skin Bleaching recalledObagi Nu-derm System Normal-oily Skin Transformation | Obagi Medical Products | Packaging Defects | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.