Fresenius Kabi USA LLC (FK USA) recalls
Fresenius Kabi USA LLC (FK USA) has 2 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 28 Aug 2013. The most frequent reason is labeling errors.
Total recalls2since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 28 Aug 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 fresenius kabi usa llc (fk usa) is recalled
Product types
By year
All fresenius kabi usa llc (fk usa) recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Irinotecan Hydrochloride Injection, 40 mg recalled | Fresenius Kabi USA LLC (FK USA) | Other | Nationwide |
| Drug | CLASS III | Calcium Gluconate Injection, USP, 10% (100 mg/mL), Single Dose Vial recalled | Fresenius Kabi USA LLC (FK USA) | Labeling Errors | 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.