FDA classifies Fresenius Kabi’s recall of Ivenix infusion pump as Class 1
Ivenix LVP, one of the three main components of the Ivenix Infusion System, is being recalled over mechanical…
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16 Jan 24
Ivenix LVP, one of the three main components of the Ivenix Infusion System, is being recalled over mechanical…
04 Dec 23
The pumps, which include BD Alaris Syringe Module, BD Alaris PCU, and Alaris PCA Module, are being recalled…
20 Nov 23
The Infusomat Space Volumetric Infusion Pump System models are being recalled by the company due to defective occlusion…
14 Sep 23
The Proclaim and Infinity IPGs were recalled due to their inability to exit magnetic resonance imaging (MRI) mode…
31 Jul 23
The TruSignal sensors were recalled because of their potential to decrease the energy delivered to the heart during…
14 Jul 23
Germany-based Draeger Medical has recalled the Oxylog 3000 Plus Emergency and Transport Ventilators over the potential risk of…
16 Jun 23
According to the FDA, the possible overheating and leakage of corrosive chemicals from the device can lead to…
25 May 23
Initiated by the medical equipment maker on 17 April 2023, the recall involves a total of 570,459 devices…
24 Apr 23
The US-based medical technology company is recalling its BALLARD ACCESS Closed Suction System for neonates and paediatrics distributed…
10 Apr 23
The Dutch medical devices maker recalled 1,088 devices in the US in February this year over the risk…