Medtronic Recalls Mahurkar Acute Dual Lumen High Flow Hemodialysis Catheters for Potential Catheter Hub Defect
A catheter hub defect may cause the Mahurkar Acute Dual Lumen High Flow Catheter to leak across the catheter’s two tubes.
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A catheter hub defect may cause the Mahurkar Acute Dual Lumen High Flow Catheter to leak across the catheter’s two tubes.
Edgewell Personal Care Company (NYSE: EPC) today expanded its voluntary nationwide recall of three batches of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 to the consumer level as outlined in the table below. One additional batch has been added to the original recall announced on July 29, 2022. A
The LifeSPARC System is being recalled because users can inadvertently cause extended pump stop. A software update will address this issue.
The LifeSPARC System is being recalled because users can inadvertently cause extended pump stop. A software update will address this issue.
Thu, 26 Jan 2023 12:02:14 -0500
RSDL Kits may leak, reducing the effectiveness of the kit when it is needed or exposing users unnecessarily to the decontamination lotion.
Blood may enter the Cardiosave IABP through a damaged balloon catheter, causing pump shut-down, or patient exposure to helium or cross-contaminated blood
2023 Medical Device Recalls
Fri, 20 Jan 2023 14:45:17 -0500
Fri, 20 Jan 2023 14:45:17 -0500
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