Devices

Device Recall ORCHESTRA/ORCHESTRA PLUS Programmer

Model / Serial
ORCHESTRA/ORCHESTRA PLUS Programmer implanted with the following pacemaker models. - REPLY Models D, DR, VDR, SR - ESPRIT Models D, DR, S, SR - FACIL Model DR1
Product Classification
General Hospital and Personal Use Devices
Device Class
Unclassified
Implanted device?
No
Distribution
Nationwide.
Product Description
ORCHESTRA/ORCHESTRA PLUS Programmer
Manufacturer
Sorin Group Italia S.r.l.
1 Event
- Recall of Device Recall ORCHESTRA/ORCHESTRA PLUS Programmer

Manufacturer

Sorin Group Italia S.r.l.

Manufacturer Address
Sorin Group Italia S.r.l., Via Crescentino, Saluggia, VC Italy
Manufacturer Parent Company (2017)
LivaNova PLC
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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