Web15 jun. 2024 · The HVAD Pump Implant Kit was classified as a Class I recall, which is the most severe type of recall. The recall states that the use of these HVAD Pump Implant Kit could cause severe injury or death. The medical devices were recalled due to a welding defect. The models affected by the recall include 1101, 1103, 1104, 1104JP, and … WebMCS1705PU: The version or model found on the device label or accompanying packaging used to identify a category or design of a device. The version or model identifies all devices that have specifications, performance, size, and composition within limits set by the labeler.
HVAD® Pump Implant Kit MCS1705PU Medical Device Identification
WebThe 1,614 affected products, model numbers 1101, 1103, 1104, 1104JP and MCS1705PU, were distributed from Oct. 11, 2006 to June 3, 2024. Devices Postmarket Safety. … WebMCS1705PU HVAD™ Pump Implant Kit 26 July 2024 Dear Physician and Healthcare Professional: Medtronic is providing this letter as a follow-up to our April 2024 … ta truck stop roanoke va
URGENT MEDICAL DEVICE NOTICE Medtronic HeartWare™ …
http://medtronicheart.com/content/dam/medtronic-com/global/HCP/Documents/clinician-letter-following-physician-no-patient-with-strain-relief-repair.pdf WebStatus: Ongoing: Mandated? Voluntary: Firm initiated: Recall Number: Z-2072-2024: Event ID: 88135: Event Description: HeartWare, HVAD Pump Implant Kit, REF MCS1705PU - Product Usage: indicated for hemodynamic support in patients with advanced, refractory left ventricular heart failure; either as a Bridge to Cardiac Transplantation (BTT), myocardial … Web3 jun. 2024 · HeartWare HVAD Implant Kit, REF MCS1705PU: Code Information: GTIN: 00888707005715, 00888707007160, 00888707007139, 00888707005364, … ta truck stop new jersey