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Displaying 1 - 7 of 7 items.
Baxter Corporation is issuing an urgent medical device correction for the Voalte Patient Safety, previously branded as Navicare Patient Safety, software versions 3.9.200 through 4.0.401. Baxter identified a potential risk where the "safety" monitoring…
RecallHealth product recall | 2023-06-02
Hillrom (a Baxter company) is issuing an urgent medical device correction for the Pro+ Mattress to inform customers of the potential for mattress top cover damage (delamination) which may result in fluid absorption in the mattress (fluid ingress).…
RecallHealth product recall | 2023-04-13
During verification testing, it was discovered that a subset of the beds under test were experiencing bent compression links when raising the head section and when maximum patient weight was simulated. This failure mode was due to a change that was made…
RecallHealth product recall | 2022-11-10
The Pro+ Mattress with Advanced Microclimate® Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned. The Pro+ hospital bed surface is a mattress…
RecallHealth product recall | 2022-07-11
With certain wireless integrations, an issue has been identified when using push button call components, normal calls, staff assist, and code calls will be moved from an active state (toning and displaying on the incoming calls…
RecallHealth product recall | 2022-06-07
The Compella bed and Compella controllers have power cords included as part of the product. Over the lifespan of each product, the respective power cord from each device can become damaged. Hillrom has received approximately one-hundred ninety-seven (197…
RecallHealth product recall | 2022-03-14
Hillrom service team has identified that during an audio station's rebooting sequence, which may occur during a system upgrade/planned service event, or with an emergency power outage, where back up power is not functioning, the audio…
RecallHealth product recall | 2021-11-26