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FDA (Device enforcement)Recalled 2024-01-05class ii

IMPULSE DYNAMICS (USA) INC: OPTIMIZER model CCM X11 implantable pulse generator (IPG) devices - Smart Mini and Lite

Hazard

OPTIMIZER devices may cease to deliver CCM therapy if the device incorrectly detects a charging error. This may cause patients to experience heart failure symptoms similar to before implantation of the device.

Details from the source

Reason for recall: OPTIMIZER devices may cease to deliver CCM therapy if the device incorrectly detects a charging error. This may cause patients to experience heart failure symptoms similar to before implantation of the device. Distribution: Domestic US distribution nationwide. International distribution to Austria Croatia Czech Republic Germany Italy Macau Poland Romania Russia Spain Sweden. Quantity: 1,469 total units Lot/code info: OPTIMIZER Smart Mini UDI-DI: 00810003380098 OPTIMIZER Lite UDI-DI: 00810003380142 All units potentially affected. The available software versions that allow the issue to manifest are 1.5.0 and 1.9.1.

UPC codes

00810003380098, 00810003380142

Source

Official record: FDA (Device enforcement)

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

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