Farmaci biosimilari in Italia: report AIFA aggiornati a novembre 2020
Italiano
The Bio-Console 560 controls a blood pump during cardiopulmonary bypass or ECMO. An electrical failure in the console may cause the pump to stop.
BD (Becton, Dickinson and Company), a leading global medical technology company, is voluntarily recalling specified lots of the ChloraPrep™ Hi-Lite Orange™ 26 mL Applicator (2% w/w chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)) to the user level due to a defective applicator.
The Tenacore Alaris Pump Bezel Assembly services and repairs Alaris infusion pump modules. Over time, the bezel repair posts may crack or separate.
On February 24th, 2021, Tenacore LLC initiated a nationwide recall of 2001 Tenacore replacement CareFusion Alaris 8100 bezels due to potentially weakened plastic. A bezel with weakened plastic may, over time, lead to separation of the bezel post (recall issue) as well as other damage to the bezel (e
The Alaris System is a fluid delivery system. The keys may become stuck or unresponsive and may lead to an infusion delay or delay in care.
Sanit Technologies LLC d/b/a Durisan announces a voluntary recall expansion of its Durisan Antimicrobial Hand Sanitizer, NonAlcohol products in various sizes listed to now include products that have not yet expired. The products are being recalled due to out of specification microbial contamination.
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