Copaxone recalls
Copaxone products have been recalled 3 times, most recently on 27 Nov 2013. The recalling company is usually Teva Pharmaceuticals USA. The most common reason is particulate matter.
Total recalls3since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 27 Nov 2013
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why copaxone is recalled
Companies
Product types
By year
All copaxone recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Copaxone (glatiramer acetate injection), 20 mg/ pre-filled syringe recalledCopaxone | Teva Pharmaceuticals U | Particulate Matter | Nationwide |
| Drug | CLASS II | Copaxone (glatiramer acetate injection), 20 mg recalledCopaxone | Teva Pharmaceuticals USA | Packaging Defects | Nationwide |
| Drug | CLASS II | Copaxone (glatiramer acetate injection), 20mg/mL recalledCopaxone | Teva Pharmaceuticals USA | Other | 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.