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FDA (Device enforcement)Recalled 2021-06-03class i

Heartware, Inc.: HeartWare HVAD Pump Implant Kit, REF 1104

Is my product affected?

HeartWare HVAD Pump Implant Kit, REF 1104

  • UPC 00888707003063
  • UPC 00888707003070
  • UPC 00888707006323
  • UPC 00888707003117
  • UPC 00888707006392
  • UPC 00888707006408
  • UPC 00888707006330
  • UPC 00888707003100
  • UPC 00888707003254
  • UPC 00888707009140
  • UPC 00888707007290
  • UPC 00888707006446
  • UPC 00888707008129
  • UPC 00888707002608
  • UPC 00888707008174
  • UPC 00888707003209
  • UPC 00888707006347

Check against the official notice below — it lists the full affected range.

What happened

Medtronic is stopping the distribution and sale of the HeartWare HVAD System, a left ventricular assist device. The company took this action based on clinical comparisons showing that the HVAD System is associated with a higher frequency of neurological adverse events and mortality compared to other commercially available left ventricular assist devices. Additionally, there have been complaints that the internal pump may delay or fail to restart.

The recall affects 943 units that were distributed worldwide, including throughout the United States and in numerous countries across Europe, the Middle East, Africa, and Asia. The record does not specify what remedy is available to affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Medtronic is stopping the distribution and sale of the HVAD System due to a growing body of observational clinical comparisons that shows a higher frequency of neurological adverse events and mortality associated with the system when compared to other commercially available left ventricular assist devices, as well as complaints that the internal pump may delay or fail to restart.

Details from the source

Reason for recall: Medtronic is stopping the distribution and sale of the HVAD System due to a growing body of observational clinical comparisons that shows a higher frequency of neurological adverse events and mortality associated with the system when compared to other commercially available left ventricular assist devices, as well as complaints that the internal pump may delay or fail to restart. Distribution: Worldwide distribution. US nationwide and Armenia, AUSTRIA, Bahrain, Belgium, CROATIA, CZECH REPUBLIC, Denmark, EGYPT, ESTONIA, FINLAND, FRANCE, GERMANY, GREECE, Hungary, Israel, ITALY, Jordan, Kazakhstan, Kuwait, Latvia, Lebanon, LITHUANIA, LUXEMBOURG, Macedonia, NETHERLANDS, Norway, POLAND, Qatar, Romania, SAUDI ARABIA, Serbia, Slovakia, SOUTH AFRICA, Spain, Sweden, SWITZERLAND, TAIWAN, Turkey, Quantity: 943 units Lot/code info: GTIN: 00888707003063, 00888707003070, 00888707006323, 00888707003117, 00888707006392, 00888707006408, 00888707006330, 00888707003100, 00888707003254, 00888707009140, 00888707007290, 00888707006446, 00888707008129, 00888707002608, 00888707008174, 00888707003209, 00888707006347 All serial numbers

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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