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Device Recall The Schiller PB 1000
Model / Serial
Patient Data Module (PDM) V2 model: Serial numbers 10.03.XXXXX
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Distribution was nationwide to medical facilities. There was also military and government distribution.
Product Description
The Schiller PB 1000, also known as: Merge Hemo Patient Data Module (PDM), V2 model, a major component of the Merge Hemo software.
Manufacturer
Merge Healthcare, Inc.
1 Event
Recall of Device Recall The Schiller PB 1000
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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
One device with a similar name
Learn more about the data
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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.
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