CARDIOHELP Emergency Drive Blockage May Impair Cardiac Blood Oxygenation
The FDA is recalling CARDIOHELP Emergency Drive units due to potential blocking that impairs blood flow. Affected patients may experience ischemia and hypoxia from inappropriate low blood oxygen.
- Product
- CARDIOHELP Emergency Drive, Part Numbers 701048002 and 701076205. The CARDIOHELP System is a blood oxygenation and carbon dioxide removal system.
- Category
- Medical Device
- Distribution
- Distributed nationwide