Hill-rom, Inc.
1069 State Route 46 East, Batesville, IN, US
Registered product codes
29 product codes
Recent MDR events
29,952 on file
- Centrella¿ BedJul 28, 2026Malfunction50053018
- ALLEN YELLOFIN HEEL STIRRUPJul 9, 2026Malfunction25762203
- PRO+Jun 17, 2026Malfunction25531774
- ALLENJun 8, 2026Malfunction25428434
- HILL-ROM CENTRELLA HOSPITAL BEDApr 29, 2026InjuryMW5187451
- CENTRELLA SMART+Apr 23, 2026Malfunction24965495
- CENTRELLA¿ BEDMar 12, 2026Injury24578808
- BAXTER MEDICAL BEDMar 11, 2026MalfunctionMW5185072
- BAXTER ENVELLA BEDJan 8, 2026MalfunctionMW5181960
- BED, AC-POWERED ADJUSTABLE HOSPITALJan 2, 2026MalfunctionMW5181580
Recalls
93 on file
- TerminatedJan 29, 2021
Multirall Q-link strap lock has not been fully engaged in the S65 rail carriage hook by user, leading to the Multirall lift becoming detached from the rail system, potentially resulting in the fall of both the lift motor and the patient
View FDA record ↗ - TerminatedOct 31, 2016
Ceiling Bracket 71 was shipped with a larger center hole. A potentially hazardous situation exists that if the Ceiling Bracket 71 with a larger center hole is used for a concrete ceiling Ultra System installation with the M8 screw and the safe working load is exceeded, the system could fall.
View FDA record ↗ - TerminatedSep 8, 2016View FDA record ↗
- TerminatedAug 9, 2016
The current construction of the side rail latch may not be able to support the full patient weight and may give way allowing the side rail to abruptly lower and the patient to fall, potentially resulting in harm. To date there has been one report of a related injury.
View FDA record ↗ - TerminatedJun 7, 2016
The center bolt of the sling bar, which connects the bar to the patient lift, has failed during use. If the sling bar is not used as intended the bolt may be weakened. If the bolt is weakened there is a potential risk for breakage with the result of a free fall of the patient. This hazard could cause potentially minor to catastrophic injuries to a patient.
View FDA record ↗ - TerminatedFeb 23, 2016
The recliners were shipped without the foot rest ottoman linkage side shields, which could result in consumer injury.
View FDA record ↗ - TerminatedNov 13, 2015
Hill-Rom is voluntarily recalling the Hill-Rom 100 Low Bed due to complaints of patient injury when exiting the beds set at the lowest position setting.
View FDA record ↗ - TerminatedJun 19, 2015
Complaints (including one reported death) allegedly of the lift arm drifting down suddenly. If the lift arm assembly is manually lifted, the actuator can become damaged and get stuck in the highest position. If a patient is lifted into the sling while the actuator is stuck, there is a potential risk of a free fall of the patient, resulting in minor or potentially catastrophic injuries.
View FDA record ↗ - TerminatedJun 19, 2015
The metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece.
View FDA record ↗ - TerminatedSep 1, 2014
The attachment latch mechanism can become bent depending on user handling. Latch mechanism bending could lead to improper engagement of the foot section and this could result in injury to the user due to a fall.
View FDA record ↗
Compliance history
Matched by FEI 1824206.
FDA inspections
2 on file
- No Action Indicated (NAI)Apr 12, 2024
Compliance: Devices
- No Action Indicated (NAI)Apr 12, 2024
Postmarket Assurance: Devices
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.