- BD Provides Update on Voluntary Recalls of Alaris™ Pump Module ...🔍
- BD Provides Update on Feb. 4🔍
- Distribution Hold of the BD Alaris™ System Update🔍
- FDA Designates Majority of BD's June 30 Alaris Pump Recall as ...🔍
- BD Provides Update on Previously Disclosed Recall of BD Alaris ...🔍
- FDA Announces Several New Recalls of BD Alaris Pump Module ...🔍
- New Urgent Medical Device Recall BD Alaris™ Pump Module ...🔍
- Becton Dickinson 🔍
BD Provides Update on Voluntary Recalls of Alaris™ Pump Module ...
BD Provides Update on Voluntary Recalls of Alaris™ Pump Module ...
In a recall notification sent on May 6, 2019External Link Disclaimer, BD confirmed that an incomplete occlusion can occur on the pumping segment ...
BD Provides Update on Feb. 4, 2020 Voluntary Recall of the ... - FDA
4, 2020 Voluntary Recall of the BD Alaris™ System PC Units and Modules ... BD Alaris™ Pump Module Model 8100, software versions 12.1.0 and ...
Distribution Hold of the BD Alaris™ System Update
BD is issuing a voluntary recall to address specific software issues with the BD Alaris™ System Infusion Pumps. ... Alaris™ representative will provide a ...
FDA Designates Majority of BD's June 30 Alaris Pump Recall as ...
BD initiated the voluntary recall to notify customers of the potential for four hardware situations that may result in the infusion pump not operating as ...
BD Provides Update on Previously Disclosed Recall of BD Alaris ...
BD initiated the voluntary recall to notify customers of the potential for four hardware situations that may result in the infusion pump not ...
FDA Announces Several New Recalls of BD Alaris Pump Module ...
The recall affects 145,492 devices of the BD Alaris Infusion Pump Module model 8100 with part numbers 49000239, 49000346, 49000438, and 49000439. The parts were ...
New Urgent Medical Device Recall BD Alaris™ Pump Module ...
BD is initiating a new voluntary recall for the BD Alaris™ Pump Module Model 8100 due to potential lifting of the keypad, which could result ...
Becton Dickinson (BD) Recalls Alaris Infusion Sets for the
• BD Provides Update on Voluntary Recalls of Alaris™ Pump Module Model 8100 and. Certain Alaris™ Pump Infusion Sets (Issued July 2019) (https ...
BD Announces FDA Classifications for August 4th Recalls of BD ...
MediaRoom · BD Alaris™ Pump Module Model 8100 (manufactured from December 1, 2016 to January 23, 2019) · Pump Module Door Assembly Replacement ...
BD Provides Update On Voluntary Recall Of Alaris Pump Modules ...
Becton, Dickinson and Co. or BD (BDX) on Thursday provided an update on two voluntary recalls related to certain Alaris Pump Modules Model ...
Medical Device Recall Notification AFFECTED DEVICES: BD Alaris ...
notifications/recall-notification-for-alaris-system-infusion-pumps). • On April 15, 2019, we initiated a recall of the BD Alaris™ Pump Module ...
BD is initiating a new voluntary recall for the BD Alaris™ Pump Module Model 8100 due to potential lifting of the keypad, which could result in one or more keys ...
BD Says Voluntary Alaris Pump Recalls Designated Class I by FDA
BD says two voluntary recalls of certain Alaris pump models has been designated Class I by the FDA.
Medical Device Recall - Updated Information Alaris™ Pump Module ...
This updated communication is being provided to expedite inspection of the affected pumps. Until the bezels affected by this recall are ...
BD provides update on voluntary recalls of Alaris Pumps
In a recall notification sent on April 15, 2019, BD informed clinicians that the bezel assemblies in the Alaris pump modules subject to this ...
On February 4, 2020, BD initiated a voluntary recall of the BD Alaris™ System to address the ... BD Alaris™ pump module model 8100. Alaris™ ...
FDA Recalls April 14 -22 | TLD Systems
BD (Becton, Dickinson and Company), a leading global medical technology company, is voluntarily recalling specified lots of the ChloraPrep™ Hi-Lite Orange™ 26 ...
BD Announces FDA Classifications for August 4th Recalls of BD ...
BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today provided an update on previously announced ...
BD Provides Update On Voluntary Recall Of Alaris Pump Modules ...
(RTTNews) - Becton, Dickinson and Co. or BD (BDX) on Thursday provided an update on two voluntary recalls related to certain Alaris Pump ...
Medical Device Recall Notification AFFECTED DEVICE: BD Alaris ...
BD Alaris™ Pump Module Model 8100, software versions 9.33 and prior ... interim, BD will offer an Alaris™ Medication Safety program for ...