Hill-Rom Recalls
38 recalls on record · December 15, 2003 to March 23, 2022 · Medical Devices, Other
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 23, 2022Medical DevicesFDA
Hill-Rom, Inc. recalls (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX co
Hazard: Traverse rail carriage delivered with non-conforming screws are too short to ensure appropriate installation. There is potential that the screws are unable to secure the traverse rail appropriately and could loosen over time causing the rail system to fall, potentially causing injury to caregivers and/or patients
February 23, 2022Medical DevicesFDA
Hill-Rom, Inc. recalls Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
Hazard: Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
February 23, 2022Medical DevicesFDA
Hill-Rom, Inc. recalls Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
Hazard: Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
December 29, 2021Medical DevicesFDA
Hill-Rom Inc. recalls These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call
Hazard: An unrecoverable error may occur where a component will fail to complete the reboot cycle, become non-functional and must be replaced.
October 6, 2021Medical DevicesFDA
Hill-Rom, Inc. recalls LikoStretch Mod 600 IC Model Number: 3156065 LikoStretch Mod 600 IC, Wide Model Number: 3156065B (obsolete since 12JUN2
Hazard: Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may fall out of the Oct lift sheet back onto the surface it is being lifted from.
October 6, 2021Medical DevicesFDA
Hill-Rom, Inc. recalls LikoStretch 1900 Model Number: 3156051 - The combination of this products allows the user to easily adjust/control the c
Hazard: Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may fall out of the Oct lift sheet back onto the surface it is being lifted from.
October 6, 2021Medical DevicesFDA
Hill-Rom, Inc. recalls Stretch Leveller Model Number: 3156200 - The combination of this products allows the user to easily adjust/control the c
Hazard: Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may fall out of the Oct lift sheet back onto the surface it is being lifted from.
October 6, 2021Medical DevicesFDA
Hill-Rom, Inc. recalls FlexoStretch Model Number: 3156057 - The combination of this products allows the user to easily adjust/control the cente
Hazard: Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may fall out of the Oct lift sheet back onto the surface it is being lifted from.
October 6, 2021Medical DevicesFDA
Hill-Rom, Inc. recalls OctoStretch with Stretch Leveller - The combination of this products allows the user to easily adjust/control the center
Hazard: Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may fall out of the Oct lift sheet back onto the surface it is being lifted from.
August 4, 2021Medical DevicesFDA
Hill-Rom, Inc. recalls Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) o
Hazard: Latch mechanism on the Lift-Off foot section of the Affinity Four Birthing Bed is damaged, it could potentially cause the installed foot section to be improperly engaged onto the bed, could result in injury to the user due to a fall.
February 10, 2021Medical DevicesFDA
Hill-Rom, Inc. recalls Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensiv
Hazard: 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
August 5, 2020Medical DevicesFDA
Hill-Rom, Inc. recalls Centrella Smart+ Bed, Catalog No. P7900 - Product Usage: intended to be used to treat or prevent pulmonary or other comp
Hazard: Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.
August 5, 2020Medical DevicesFDA
Hill-Rom, Inc. recalls Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complicatio
Hazard: Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.
June 10, 2020Medical DevicesFDA
Hill-Rom, Inc. recalls Centrella Smart+ Bed, Catalog Number P7900
Hazard: The Bed Exit System may fail to send a remote alert through the nurse call system if a remote alert was previously sent and cancelled at the in-room nurse call wall unit.
April 1, 2020Medical DevicesFDA
Hill-Rom Inc. recalls NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient Safety (Patient Safety) Software is c
Hazard: There is a software issue which may result in failure to monitor or control patient's bed exit mechanism.
April 18, 2018Medical DevicesFDA
Hill-Rom, Inc. recalls Progressa Bed - AC-powered adjustable hospital bed
Hazard: A component used within the braking system may break resulting in one or more brake pedals on the bed staying in brake or not being engaged which could result in unwanted bed movement and possible patient or user injury.
April 19, 2017Medical DevicesFDA
Hill-Rom, Inc. recalls TotalCare Bed Systems, Model Numbers P1900, PR1900, and U1900 with 3-Level Patient Position Monitoring and Scale Upgrad
Hazard: The bed exit alarm may not function properly if the alarm has been armed for a period longer than seventy-two (72) hours without the alarm being triggered by patient movement or removal of patient weight within that time period.
November 9, 2016Medical DevicesFDA
Hill-Rom, Inc. recalls Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likora
Hazard: 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.
September 14, 2016Medical DevicesFDA
Hill-Rom, Inc. recalls Affinity Four Birthing Bed Model P3700 The primary packaging is pictured below, and utilizes a metal packing brace,
Hazard: FDA Class II
August 17, 2016Medical DevicesFDA
Hill-Rom, Inc. recalls Volker 2080, 2082, S 280 and S 282 series beds with lateral release button. A/C Powered Adjustable Hospital Bed Prod
Hazard: 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.
June 15, 2016Medical DevicesFDA
Hill-Rom, Inc. recalls Liko Universal SlingBars Universal SlingBar" 350, Universal SlingBar" 350 QRH, Universal SlingBar" 350 R2R, Uni
Hazard: 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.
March 2, 2016Medical DevicesFDA
Hill-Rom, Inc. recalls Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to pr
Hazard: The recliners were shipped without the foot rest ottoman linkage side shields, which could result in consumer injury.
November 25, 2015Medical DevicesFDA
Hill-Rom, Inc. recalls Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed
Hazard: 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.
July 1, 2015Medical DevicesFDA
Hill-Rom, Inc. recalls Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
Hazard: The metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece.
June 24, 2015Medical DevicesFDA
Hill-Rom, Inc. recalls Viking M, L, and XL Mobile Lifts. Non-AC-powered patient lift.
Hazard: 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.
September 10, 2014Medical DevicesFDA
Hill-Rom, Inc. recalls Affinity¿ Four Birthing Bed, Product Usage: Product is intended to be used as birthing beds for women of child bear
Hazard: 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.
July 31, 2013Medical DevicesFDA
Hill-Rom, Inc. recalls TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum Complete mattress, and AccuMax Quantum Convertible
Hazard: When the bed is put into the chair egress position, the magnets on the mattress may not hold the bottom of the mattress flat to the bed frame, and the mattress foot section will extend away from the bed at an angle. A patient attempting to get back into the bed may miss the seat and sit on the foot section instead. The patient can slide down to the floor, or fall, with possible injury.
June 12, 2013Medical DevicesFDA
Hill-Rom, Inc. recalls SlingBar Standard. Designed to meet the needs for lifting humans.
Hazard: Retrospective review found 4 sling bars that may present a potential for impalement if a patient, caregiver or bystander were to fall onto the hooks based on a simulated test method. In effort to eliminate any risk of injury, Hill-Rom is requesting products be removed from field use and replaced with an updated design.
June 12, 2013Medical DevicesFDA
Hill-Rom, Inc. recalls SlingBar Wide 670. Designed to meet the needs for lifting humans.
Hazard: Retrospective review found 4 sling bars that may present a potential for impalement if a patient, caregiver or bystander were to fall onto the hooks based on a simulated test method. In effort to eliminate any risk of injury, Hill-Rom is requesting products be removed from field use and replaced with an updated design.
June 12, 2013Medical DevicesFDA
Hill-Rom, Inc. recalls SlingBar 360. Designed to meet the needs for lifting humans.
Hazard: Retrospective review found 4 sling bars that may present a potential for impalement if a patient, caregiver or bystander were to fall onto the hooks based on a simulated test method. In effort to eliminate any risk of injury, Hill-Rom is requesting products be removed from field use and replaced with an updated design.