Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1774-2018 — Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for providing short-term hemodynamic support in patients with advanced refractory left ventricular heart failure.

U.S. FDA — Device Enforcement · United States · 2018-04-05 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1774-2018
Date of alert
2018-04-05
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Abbott
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00813024013297
Reported risk: Reports of outflow graft twist occlusions. Patients whose devices experience outflow graft occlusions will experience a persistent low flow alarm. Outflow graft occlusions can result in serious adverse events such as hemodynamic compromise, thrombus, and death.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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