Terumo Cardiovascular Systems Corporation - Terumo Cardiovascular Procedure Kits - Class 2 Recall
Cardiovascular Procedure Kits that include High Crack Check Valve PN 205307A Part Number: 6375 16010 62974 65246 66312 66342 66388 66650 66852 70472 74307 74365 74366 74430 74475 74477 74502 74773 74873 75065 75157 75195 75409 75410 75473 75533 75534 75607 75765 75797 75833 75903 75956 75973 76131 76178 76278 76306 76398 76427 76498 76519 76536 76565 76575 76628 76630 76635 76644 76687 76725 76775 76789 76832 76839 76878 76900 76999 77010 77014 77015 77105 77227 77299 77304 77305 77412 77450 77496 77516 77629 77722 77742 77757 77791 77794 77796 78018 78027 165720 205307A 65046-03 65080-06 65167-06 65934-01 65940-01 66041-0...
Source: Medical Device Recalls - March 30, 2024 Category: Medical Devices Source Type: alerts
Abiomed, Inc. - Automated Impella Controller (AIC) - Class 2 Recall
Automated Impella Controller (AIC), Product No. 0042-0000-US, 0042-0010-US, 0042-0040-US. Used with Impella Ventricular Support Systems (cardiovascular) (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 23, 2024 Category: Medical Devices Source Type: alerts
Maquet Medical Systems USA - ROTAFLOW - Class 2 Recall
BO-RF-32-USA RotaFlow Centrifugal Pump with SOFTLINE Coating, Product Code 701047553. For use with an extracorporeal cardiovascular or cardiopulmonary bypass circuit. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 3, 2024 Category: Medical Devices Source Type: alerts
Maquet Medical Systems USA - ROTAFLOW - Class 2 Recall
BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating, Product Code 701047554. For use with an extracorporeal cardiovascular or cardiopulmonary bypass circuit. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 3, 2024 Category: Medical Devices Source Type: alerts
American Contract Systems, Inc. - Custom procedural convenience kits and trays - Class 2 Recall
Procedural convenience kits and trays, cardiac, labeled as: a) EP LAB BI V IMPLANT PACK, kit number AGBI64J; b) LAB DEVICE IMPLANT, kit number AGDI40J; c) LAB DEVICE IMPLANT, kit number AGDI40K; d) MINOR VASCULAR, kit number AGMV26O; e) OPEN HEART ACCESSORY, kit number AGOH98Q; f) OPEN HEART ACCESSORY, kit number AGOH98R; g) OPEN HEART ACCESSORY, kit number AGOH98S; h) PERIPHERAL VASCULAR, kit number AGPV28O; i) PERIPHERAL VASCULAR, kit number AGPV28P; j) MINOR VASCULAR, kit number AHMV26J; k) MINOR VASCULAR, kit number AHMV26K; l) HEART PACK - 205947, kit number ANCV78AX; m) HEART PACK - 205947 , kit number A...
Source: Medical Device Recalls - January 27, 2024 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Atrium Express Dry Suction Dry Seal Chest Drain - Class 1 Recall
Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 13, 2024 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Atrium Express Dry Suction Dry Seal Chest Drain - Class 1 Recall
Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 13, 2024 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Vasoview Hemopro - Class 2 Recall
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 13, 2024 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Vasoview Hemopro - Class 2 Recall
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W . (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 13, 2024 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Acrobati Vacuum Positioner System - Class 2 Recall
Acrobat-i Vacuum Positioner System, Model Number XP-5000Z (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 20, 2023 Category: Medical Devices Source Type: alerts
ROi CPS LLC - Regard - Class 2 Recall
Regard CV PK, Item Numbers a) 880289014, b) 880289015; cardiovascular convenience kit (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 17, 2023 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Vasoview 6 Pro - Class 2 Recall
Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2). (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 3, 2023 Category: Medical Devices Source Type: alerts
Maquet Cardiovascular, LLC - Maquet Getinge - Class 2 Recall
Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a sternotomy incision approach. Product Code: OM-10000Z (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 23, 2023 Category: Medical Devices Source Type: alerts
CARDIOVASCULAR FORMULA (cactus grandiflorus, spigelia anthelmia, kalmia latifolia, arsenicum album, strophanthus hispidus, scilla maritima, digitalis purpurea, phosphorus, kali carbonicum) spray [Nutritional Specialties, Inc.]
Updated Date: Mon, 25 Sep 2023 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 25, 2023 Category: Drugs & Pharmacology 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. OPEN HEART CDS-LF, Model Number: CDS840451L; b. OPEN HEART LINE SET UP, Model Number: DYNJ908179, DYNJ908179A; c. OPEN HEART PACK, Model Number: DYNJ43741B, DYNJ66216, DYNJ66216A, DYNJ66216B, DYNJ66216C; d. OPEN HEART PACK A B, Model Number: DYNJ53984G; e. OPEN HEART PACK A & B, Model Number: DYNJ0283397T, DYNJ0283397U, DYNJ53984F, DYNJ53984G; f. OPEN HEART PACK-LF, Model Number: DYNJ0371669N; g. OPEN HEART PACK-RF-LF, Model Number: DYNJ22232W; h. OPEN HEART PART 2, Model Number: DYNJ901075O, DYN...
Source: Medical Device Recalls - August 4, 2023 Category: Medical Devices Source Type: alerts
