FDA classifies LivaNova’s recall of LifeSPARC system’s controller as Class I
The US health regulator claimed that the device could reach critical failure mode due to a problem in…
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30 Jan 23
The US health regulator claimed that the device could reach critical failure mode due to a problem in…
22 Dec 22
The tests were performed to assess potential health risks with the polyester-based PE-PUR sound abatement foam in specific…
24 Nov 22
The recall is based on reports of interference to other nearby critical medical devices by radiofrequency emissions from…
22 Nov 22
The firm has notified the two issues to the appropriate authorities throughout the world and anticipates finishing its…
25 Oct 22
The Dutch health technology company has been hit with a loss of €1.5bn in Q3 2022, which was…
10 Oct 22
The recall list includes 17 versions of the reusable metal containers, sold under the Genesis Sterrad brand, which…
16 Sep 22
The Clearlink Basic Solution Set with Duovent is being recalled after increased customer reports of leaks that may…
30 Aug 22
The US FDA said that the machines may contain plastic contaminated with a non-compatible material that could leak…
26 Aug 22
The firm recalled the HeartWare Ventricular Assist Device (HVAD) system batteries due to risks of electrical faults that…
29 Jun 22
The CARESCAPE R860 ventilator's backup batteries and replacement backup batteries were recalled as they were draining fast and…