Arjo recalls
Arjo has 9 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 19 Jul 2017.
Total recalls9since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 19 Jul 2017
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 9 100%Class III 0 0%
Why arjo is recalled
Product types
By year
All arjo recalls, newest first
9 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | ArjoHuntleigh Flowtron ACS900, medical pump recalled | Arjo | Device Malfunction | Nationwide |
| Device | CLASS II | The Concerto Basic Shower Trolley is intended recalled by Arjo | Arjo | Other | 36 states |
| Device | CLASS II | Medium 2-Hooks Spreader Bar for use with Loop Slings recalled by Arjo | Arjo | Other | 5 states |
| Device | CLASS II | Enterprise 9000 Bed recalled by Arjo | Arjo | Device Malfunction | Nationwide |
| Device | CLASS II | Enterprise 8000 Bed recalled by Arjo | Arjo | Other | Nationwide |
| Device | CLASS II | Flowtron Trio DVT Pump recalled by Arjo | Arjo | Other | Nationwide |
| Device | CLASS II | Encore Mobile Patient Lifter recalled by Arjo | Arjo | Foreign Material | Nationwide |
| Device | CLASS II | Sara Plus Mobile Patient Lifter recalled by Arjo | Arjo | Foreign Material | Nationwide |
| Device | CLASS II | Chorus Mobile Patient Lifter recalled by Arjo | Arjo | Foreign Material | 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.