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Devices
Device Recall RENEWAL 3 DS HE ICD
Model / Serial
508822, 508827 and 508862
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
CA, IL, MI, MO, OR and PA
Product Description
CONTAK RENEWAL 3 DS HE, model H177 CRT-D Cardiac Resynchronization Therapy Defibrillator. Contents have been Sterilized with gaseous ethylene oxide. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA. Provides ventricular tachyarrhythmia and cardiac resynchronization therapies.
Manufacturer
Guidant Corporation
1 Event
Recall of Device Recall RENEWAL 3 DS HE ICD
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Manufacturer
Guidant Corporation
Manufacturer Address
Guidant Corporation, 4100 Hamline Ave N, Saint Paul MN 55112-5700
Source
USFDA
Language
English
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