Devices

Device Recall PADPRO DULT Radiotranslucent Pad w/Zoll connector

Model / Serial
Lots Y040605-1, Y040605-2, Y052605-4, Y120805-2, Y111605-3, Y092805-6, Y010506-10, Y010506-9.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Canada, Romania, Chile, and Belgium
Product Description
PADPRO ADULT Radiotranslucent Pad w/Zoll¿ connector. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes, REF/Catalog # 2516Z. RX ONLY. Made in USA for: CONMED CORPORATION Utica, New York, 13502.
Manufacturer
Conmed Corporation
1 Event
- Recall of Device Recall PADPRO DULT Radiotranslucent Pad w/Zoll connector

Manufacturer

Conmed Corporation

Manufacturer Address
Conmed Corporation, 525 French Road, Utica NY 13502-5945
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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