Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175728AP0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft01 Branch, Product Code: M00202175834P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175822P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175730AP0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175914P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175912P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175926P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175928P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175820P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175832P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175732P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - HEMASHIELD PLATINUM WOVEN/MICROVEL DOUBLE VELOUR VASCULAR GRAFTS - Class 2 Recall
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175828P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 5, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - Phillips Azurion 7 M20 - Class 2 Recall
Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079 Image guidance in diagnostic, interventional and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular, cardiovascular and neuro procedures. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 25, 2020 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular Us Sales, Llc - Avalon Elite Vascular Access Kit - Class 2 Recall
Avalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 28, 2020 Category: Medical Devices Source Type: alerts
QUIDEL CARDIOVASCULAR INC - Triage TOX Drug Screen Control 1 - Class 2 Recall
Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel Cardiovascular Inc. 9975 Summers Ridge Road San Diego, CA 92121 USA Quidel.com (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 21, 2020 Category: Medical Devices Source Type: alerts
