Obagi Medical Products recalls
Obagi Medical Products has 1 recall on record with the FDA and USDA, the earliest in 2014 and the latest reported on 12 Nov 2014. The most frequent 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 medical products is recalled
Product types
By year
All obagi medical products 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.