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Tenacore Recalls Alaris Pump Bezel Assembly and Alaris Infusion Pumps repaired with Bezel Assembly Due to Possible Cracked or Separated Bezel Repair Posts

The Tenacore Alaris Pump Bezel Assembly services and repairs Alaris infusion pump modules. Over time, the bezel repair posts may crack or separate.

http://www.fda.gov/medical-devices/medical-device-recalls/tenacore-recalls-alaris-pump-bezel-assembly-and-alaris-infusion-pumps-repaired-bezel-assembly-due

 
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Tenacore LLC Issues Nationwide Recall of Tenacore’s Replacement for the Front Bezel Assembly of the CareFusion Alaris 8100 Infusion Pump Module

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

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tenacore-llc-issues-nationwide-recall-tenacores-replacement-front-bezel-assembly-carefusion-alaris

 
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Medtronic Recalls HeartWare HVAD Battery Cables, Data Cables, Adapter Cables and Controller 2.0 Ports Due to Risk of Damage to Controller Ports

The HeartWare HVAD System pump is used in patients with heart failure. Some pumps may stop because of damaged controller ports

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-heartware-hvad-battery-cables-data-cables-adapter-cables-and-controller-20-ports

 
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Durisan Announces a Voluntary Recall Expansion of its Antimicrobial Hand Sanitizer

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.

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/durisan-announces-voluntary-recall-expansion-its-antimicrobial-hand-sanitizer