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 month

Severity split

Class I 0 0%Class II 9 100%Class III 0 0%

Why arjo is recalled

By year

All arjo recalls, newest first

9 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIArjoHuntleigh Flowtron ACS900, medical pump recalledArjoDevice MalfunctionNationwide
DeviceCLASS IIThe Concerto Basic Shower Trolley is intended recalled by ArjoArjoOther36 states
DeviceCLASS IIMedium 2-Hooks Spreader Bar for use with Loop Slings recalled by ArjoArjoOther5 states
DeviceCLASS IIEnterprise 9000 Bed recalled by ArjoArjoDevice MalfunctionNationwide
DeviceCLASS IIEnterprise 8000 Bed recalled by ArjoArjoOtherNationwide
DeviceCLASS IIFlowtron Trio DVT Pump recalled by ArjoArjoOtherNationwide
DeviceCLASS IIEncore Mobile Patient Lifter recalled by ArjoArjoForeign MaterialNationwide
DeviceCLASS IISara Plus Mobile Patient Lifter recalled by ArjoArjoForeign MaterialNationwide
DeviceCLASS IIChorus Mobile Patient Lifter recalled by ArjoArjoForeign MaterialNationwide

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.