FDA classifies Avanos’ recall of BALLARD ACCESS Closed Suction Systems as Class I
The US-based medical technology company is recalling its BALLARD ACCESS Closed Suction System for neonates and paediatrics distributed…
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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…
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…