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Datascope/Maquet/Getinge Recalls Cardiosave Hybrid and...

10 August 2023
Datascope/Maquet/Getinge recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) for unexpected electrical shutdowns.

Dräger Issues Worldwide Voluntary Recall Notification...

7 August 2023
Drägerwerk AG & Co. KGaA initiated a voluntary recall notification for Dräger Carina Sub-Acute Care Ventilators to address possible contamination of the breathing gas with 1,3-Dichloropropan-2-ol, a constituent of the PE-PUR foam used for sound insulation. To date, Dräger’s market surveillance act

Baxter Healthcare Corporation Recalls SIGMA Spectrum...

31 July 2023
Software upgrades to the SIGMA Spectrum and Spectrum IQ infusion pumps are leading to an increase in false alarms for upstream occlusion.

Lupin Pharmaceuticals, Inc. Issues Voluntary Nationwide...

31 July 2023
Lupin Pharmaceuticals Inc. (Lupin) is voluntarily recalling two (2) lots of Tydemy (Drospirenone, Ethinyl Estradiol and Levomefolate Calcium Tablets 3mg/0.03mg/0.451 mg and Levomefolate Calcium Tablets 0.451 mg) to the patient (consumer/user) level due to out of specification (OOS) test results at t

Baxter Issues Urgent Medical Device Correction for...

31 July 2023
Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for Spectrum V8 and Spectrum IQ infusion pumps in the U.S. and Puerto Rico that have been upgraded to software versions v8.01.01 and v9.02.01. The Correction is due to an increase in reported false upstream o
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