Paclitaxel recalls
Paclitaxel products have been recalled 2 times, most recently on 4 Dec 2013. The recalling company is usually Hospira. The most common reason is packaging defects.
Total recalls2since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 4 Dec 2013
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 50%Class III 1 50%
Why paclitaxel is recalled
Companies
Product types
By year
All paclitaxel recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Paclitaxel Injection, USP (semisynthetic) recalled by Fresenius Kabi USAPaclitaxel | Fresenius Kabi USA | Packaging Defects | Nationwide |
| Drug | CLASS II | Paclitaxel Injection, 6 mg/mL Single Dose Vial recalled by HospiraPaclitaxel | Hospira | Particulate Matter | 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.