Hill-Rom recalls

Hill-Rom has 37 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 23 Mar 2022. 7 are still ongoing.

Total recalls37since 2012
Last 12 months0reported
Class I13% of total
Ongoing7latest 23 Mar 2022

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 3%Class II 36 97%Class III 0 0%

By year

Ongoing hill-rom recalls

7 active
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IILiko Mobile Lifts: Primarily intended for use recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IILiko Mobile Lifts: Primarily intended for use recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IIOctoStretch with Stretch Leveller recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IIFlexoStretch Model Number recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IIStretch Leveller recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IILikoStretch 1900 Model Number: 3156051 - The combination of this recalledHill-RomOtherNationwide

All hill-rom recalls, newest first

37 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IITraverse Rail Carrier E-System recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IILiko Mobile Lifts: Primarily intended for use recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IILiko Mobile Lifts: Primarily intended for use recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IIThese are communication systems, labeled as recalled by Hill-RomHill-RomDevice MalfunctionNationwide
DeviceCLASS IIOctoStretch with Stretch Leveller recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IIFlexoStretch Model Number recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IIStretch Leveller recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IILikoStretch 1900 Model Number: 3156051 - The combination of this recalledHill-RomOtherNationwide
DeviceCLASS IILikoStretch Mod 600 IC recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IIAffinity Four Birthing Bed-used as a birthing bed recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS ILiko Multirall 200 overhead lift- overhead lift recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IICentrella Smart+ Bed recalled by Hill-RomHill-RomDevice MalfunctionNationwide
DeviceCLASS IIProgressa Bed recalled by Hill-RomHill-RomDevice MalfunctionNationwide
DeviceCLASS IICentrella Smart+ Bed recalled by Hill-RomHill-RomDevice MalfunctionNationwide
DeviceCLASS IINaviCare Patient Safety recalled by Hill-RomHill-RomDevice Malfunction11 states
DeviceCLASS IIProgressa Bed - AC-powered adjustable hospital bed recalled by Hill-RomHill-RomDevice MalfunctionNationwide
DeviceCLASS IITotalCare Bed Systems recalled by Hill-RomHill-RomDevice MalfunctionNationwide
DeviceCLASS IIProduct Number 3102071 Ceiling Bracket, Arch 71 White recalledHill-RomOther4 states
DeviceCLASS IIAffinity Four Birthing Bed recalled by Hill-RomHill-RomForeign Material16 states
DeviceCLASS IIVolker 2080, 2082, S 280 and S 282 series beds recalled by Hill-RomHill-RomDevice MalfunctionNationwide
DeviceCLASS IILiko Universal SlingBars Universal SlingBar" recalled by Hill-RomHill-RomDevice MalfunctionNationwide
DeviceCLASS IIBariatric Power Recliner, Product recalled by Hill-RomHill-RomOther39 states
DeviceCLASS II100 Low Bed (GPAC) AC Powered adjustable hospital bed recalledHill-RomOtherNationwide
DeviceCLASS IISteriseal-Cannula Ophthalmic recalled by Hill-RomHill-RomForeign MaterialNationwide
DeviceCLASS IIViking M, L, and XL Mobile Lifts recalled by Hill-RomHill-RomOther11 states
DeviceCLASS IIAffinity¿ Four Birthing Bed recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IITotalCare Bed used with AccuMax Quantum VPC mattress recalledHill-RomDevice MalfunctionNationwide
DeviceCLASS IISlingBar Wide recalled by Hill-RomHill-RomOtherNationwide
DeviceCLASS IISlingBar 360. Designed to meet the needs for lifting humans recalledHill-RomOtherNationwide
DeviceCLASS II1000 Bed, Product No. P1160 recalled by Hill-RomHill-RomOtherNationwide

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.