Devices

Device Recall The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM),

Model / Serial
All Schiller PB-1000 PDM's distributed on or before 8/11/2016.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Distribution US nationwide.
Product Description
The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM), a major component of the Merge Hemo software.
Manufacturer
Merge Healthcare, Inc.
1 Event
- Recall of Device Recall The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM),

Manufacturer

Merge Healthcare, Inc.

Manufacturer Address
Merge Healthcare, Inc., 900 Walnut Ridge Dr, Hartland WI 53029-8347
Manufacturer Parent Company (2017)
International Business Machines Corp.
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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