Animas recalls
Animas has 6 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 11 Feb 2015. The most frequent reason is device malfunction.
Total recalls6since 2012
Last 12 months0reported
Class I117% of total
Ongoing0latest 11 Feb 2015
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 17%Class II 4 67%Class III 1 17%
Why animas is recalled
Product types
By year
All animas recalls, newest first
6 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Vibe Insulin Infusion Pump recalled by Animas | Animas | Device Malfunction | PA |
| Device | CLASS II | Vibe Insulin Infusion Pump recalled by Animas | Animas | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | Vibe Insulin Infusion Pump and System recalled by Animas | Animas | Other | PA |
| Device | CLASS I | Animas(R) 2020 Insulin Infusion Pump recalled | Animas | Device Malfunction | Nationwide |
| Device | CLASS III | Animas(R) IR 1200 Insulin Infusion Pumps Indicated recalled | Animas | Device Malfunction | Nationwide |
| Device | CLASS II | IR1200, IR1250(IR1200 Plus) recalled by Animas | Animas | Lead & Heavy Metals | 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.