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.
June 12, 2013Medical DevicesFDA
Hill-Rom, Inc. recalls SlingBar 350. 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 Hill-Rom 1000 Bed, Product No. P1160. The Hill-Rom 1000 Bed is intended for low to moderate acuity patient in the medi
Hazard: Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame.
March 20, 2013Medical DevicesFDA
Hill-Rom, Inc. recalls TotalCare SpO2RT2 bed. Product Usage: Bed, flotation therapy, powered bed may be used in a variety of settings in
Hazard: In certain situations a software problem with the TotalCare SpO2RT¿ 2 bed may occur that can lead to inadvertent loss of sufficient surface cushion pressure to adequately support the patient. This may increase the likelihood of skin irritation for patients at higher risk of developing pressure-related skin conditions. A correction to the software program is currently being developed and tested,
February 27, 2013Medical DevicesFDA
Hill-Rom, Inc. recalls Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and
Hazard: Liko/Hill-Rom to date has received two reports from facilities alleging that the overhead rail system has failed to the extent that the overhead rails have fallen down while in use in high humidity (swimming pool) areas. Analysis of the incidents suggest that the components (hardware) used to secure the rail to the ceiling had corroded and may be unsuitable for environments with an atmosphere con
January 9, 2013Medical DevicesFDA
Hill-Rom, Inc. recalls Liko Standard Slingbar 450. The Standard Slingbar 450 is a versatile sling bar which can be used for most lifting sit
Hazard: Liko/Hill-Rom has received reports from facilities which indicate that serious injuries have been received related to the Standard Sling bar 450. There have been 6 complaints of injury related to the product over the past 32 years (6 out of 838,687,856 estimated patient uses). One of the injuries was associated with a patient during use, four injuries occurred when the slingbar was not in use wher
August 1, 2012Medical DevicesFDA
Hill-Rom, Inc. recalls Affinity Four Birthing Bed P3700 Product Usage: The Affinity, Four Birthing Bed is intended to be used as birthing
Hazard: During review of our last braking system via that field corrective action, the system still did not meet our expectations, which is to eliminate the hazards of patient falling. Bed movement immediately prior to, or during the birthing process may still create distractions and delays, resulting in patient or caregiver falls, or contribute to a deviation in a procedure, (e.g. IV insertion, epidural
July 4, 2012Medical DevicesFDA
Hill-Rom, Inc. recalls Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the
Hazard: During an evaluation of Advanta 2 siderail samples returned from the field it was found that the screws used to attach the siderail were being stripped from the plastic cavity of the siderail.
December 15, 2003OtherCPSC
CPSC, Hill-Rom Announce Recall of Rocking Chairs
Hazard: The chairs' support assembly can fail and cause the rocking chair to collapse, posing the risk of injury to the user.