Cardinal Health 200, LLC - Presource - Class 2 Recall
Procedure packs: (1) Presource PBDS, Cat. PC71EXOU7, Ohio State Univ Wexner Med Ctr, Kit, Extraction Ross, Sterile; (2) Presource PBDS, Cat. PVOCMVBLC, Bellevue Hospital Center, Kit, Endovascular. (3) Presource PBDS, Cat. PVRMMVAOH7, Regional Medical Center of, Kit, Dr. Ross Minor Vascular, Sterile; (4) Presource PBDS, Cat. PV30VPUHA, Univ Hlth Net Toronto Gen Hosp, Kit, Tavi, Sterile; (5) Presource Cat Pack, Cat. SANOCCPDM2, DMAC Vascular Lab LLC, Sterile; (6) Presource Pacemaker Pack, Cat. SAN1FPMULM, U of L Health, Sterile; (7) Presource OR Angio Pack, Cat. SAN11OADMM, Suny Downstate, Sterile; (8) Presource Device Impl...
Source: Medical Device Recalls - October 11, 2023 Category: Medical Devices Source Type: alerts
MEDLINE INDUSTRIES, LP - Northfield - Class 2 Recall
Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. DR. ROSEN VEIN PACK, Model Number: DYNJ67517; b. DR. VANBOSSE LOWER EXT PACK, Model Number: DYNJ51416B; c. DRAINAGE TRAY, Model Number: DYNJ42913, DYNJ42913A; d. ECMO PACK, Model Number: DYNJ61243; e. EGG RETRIEVAL PACK, Model Number: DYNJ66291, DYNJ66291A; f. EH TAVR PACK, Model Number: DYNJ57449A; g. ELVS PACK-LF, Model Number: DYNJ26940G; h. ENDO AAA HYBRID CHRG, Model Number: DYNJ60126; i. ENDOVASCULAR OR PACK, Model Number: DYNJ54265; j. ENDOVASCULAR PACK, Model Number: DYNJ59085; k. ENDOVA...
Source: Medical Device Recalls - August 4, 2023 Category: Medical Devices Source Type: alerts
Medtronic Vascular, Inc. - Valiant Navion Thoracic Stent Graft System - Class 1 Recall
Valiant Navion Thoracic Stent Graft System. For endovascular repair of lesions in the descending thoracic aorta (DTA). (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 11, 2021 Category: Medical Devices Source Type: alerts
Cook Inc. - Zenith Alpha Abdominal Endovascular Graft - Class 2 Recall
Zenith Alpha Abdominal Endovascular Graft, Catalog Prefix ZIMB - Product Usage: is indicated for the endovascular treatment of patients with abdominal aortic or aorto-iliac aneurysms having morphology suitable for endovascular repair. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 10, 2020 Category: Medical Devices Source Type: alerts
W L Gore & Associates, Inc. - GORE TAG Conformable Thoracic Stent Graft with ACTIVE CONTROL System - Class 2 Recall
Conformable Thoracic Stent Graft, Rx only, Sterile EO - Product Usage: This device is intended for endovascular repair of lesions of the descending thoracic aorta. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 21, 2020 Category: Medical Devices Source Type: alerts
W L Gore & Associates, Inc. - GORE TAG(R), THORACIC ENDOPROSTHESIS, CONFORMABLE - Class 2 Recall
GORE(R) TAG(R), THORACIC ENDOPROSTHESIS, CONFORMABLE. The GORE(R) TAG(R) Thoracic Endoprosthesis is intended for endovascular repair of all lesions of the descending thoracic aorta. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 26, 2017 Category: Medical Devices Source Type: alerts
W L Gore & Associates, Inc. - GORE TAG, THORACIC ENDOPROSTHESIS, CONFORMABLE - Class 2 Recall
GORE TAG, THORACIC ENDOPROSTHESIS, CONFORMABLE. The GORE TAG Thoracic Endoprosthesis is intended for endovascular repair of all lesions of the descending thoracic aorta. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 26, 2017 Category: Medical Devices Source Type: alerts
Cook Medical Incorporated - Zenith Alpha Thoracic Endovascular Graft - Class 1 Recall
Zenith Alpha Thoracic Endovascular Graft The Zenith Alpha" Thoracic Endovascular Graft is indicated for the endovascular treatment of patients with isolated lesions of the descending thoracic aorta (not including dissections) having vascular anatomy suitable for endovascular repair including: " Iliac/femoral anatomy that is suitable for access with the required introduction systems, " Nonaneurysmal aortic segments (fixation sites) proximal and distal to the thoracic lesion: " with a length of at least 20 mm, and " with a diameter measured outer wall to outer wall of no greater than 42 mm and no le...
Source: Medical Device Recalls - August 11, 2017 Category: Medical Devices Source Type: alerts
