Alaris recall update
WebOn Aug. 4, 2024, BD recalled 305,526 BD Alaris PC Unit 8015 models and keypad replacement kits manufactured from April 7, 2024 to June 15, 2024. The company recalled the devices because one or more keys on the keypad could become stuck or unresponsive. This could prevent clinicians from changing medication or fluid infusions and infusion delay. WebAug 20, 2024 · BD Provides Update on Previously Disclosed Recall of BD Alaris System Hardware Majority of June 30 Recall Designated as Class I Recall by FDA
Alaris recall update
Did you know?
WebMay 3, 2024 · The FDA has identified the recall of the Alaris Infusion Pump Module 8100 Bezel as a Class I recall, the most serious type. Use of these devices may cause serious injuries or death. This recall applies to the Alaris Infusion Pump Module Model 8100 Front Bezel purchased and/or installed by Pacific Medical Group (DBA Avante Health …
WebJul 29, 2024 · for the February 4, 2024 BD Alaris™ System1 recall through a new version of software. The February 4, 2024 voluntary recall action notified customers of the following areas where the infusion ... BD expressly disclaims any undertaking to update any forward-looking statements set forth herein to reflect events or circumstances after the date ... WebJul 27, 2024 · BD Alaris™ System Software Update to Address Class I Software Recall . On February 4 , 2024, BD initiated a recall of the Alaris™ System that addressed …
WebSep 23, 2024 · The fourth recall involving BD Alaris EtCO2 Module 8300 models manufactured from January 5, 2024 to January 4, 2024 was given a Class II designation. These devices were found to contain an... WebJul 18, 2024 · Information about this recall, including the original and updated recall notification, is available on BD's website at alaris.bdproductnotice.com or call BD at 888-562-6018. Alaris™ Infusion Sets
WebApr 16, 2024 · CareFusion 303, Inc. Recalls BD Alaris Pump Module Model 8100 Due to Risk of Stuck or Unresponsive Keys The FDA has identified this as a Class I recall, the most serious type of recall....
WebOver the years, BD has issued several recalls for its Alaris System infusion pumps. In 2024 alone, the company issued four recalls affecting more than one million devices sold in … how far is chiefland fl from ocala flWebAug 2, 2024 · Under U.S. Food and Drug Administration (FDA) guidance, BD will release Alaris™ System software version 12.1.2 and associated ancillary software to remediate the affected software. Effective... higgins and coWebJul 29, 2024 · for the February 4, 2024 BD Alaris™ System1 recall through a new version of software. The February 4, 2024 voluntary recall action notified customers of the following … how far is chiefland from gainesvilleWebFeb 4, 2024 · Under U.S. Food and Drug Administration (FDA) guidance, BD will release Alaris™ System software version 12.1.2 and associated ancillary software to … higgins and burke tea k cupsWebFeb 6, 2024 · The Alaris systems are used in care of 70% of patients who are on infusion pump therapy, BD said. The company reported on a call with investors in November it was planning upgrades to the pump systems, including … higgins and higgins leaving cert musicWebJul 18, 2024 · Customers should continue to refer to the attachments included in the recall notification issued on April 15, 2024. Information about this recall, including the original and updated recall... how far is chicopee ma from boston maWebAug 3, 2024 · On March 6, 2024, the U.S. Food and Drug Administration announced that it had classified the Becton Dickinson Alaris System infusion pump recall as a Class I recall, the agency’s most severe recall for medical devices that could cause serious injury or death. how far is chiefland from orlando