Devices

Device Recall PadPak and PediPak accessories for the HeartSine SamaritanPAD 300P and 350P device

Model / Serial
Pad-Pak 01 & Pad-Pak 02 ¿ Adult Lot Numbers: A1785 to A1805 ¿ Pediatric Lot Numbers: P433 to P445.
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Worldwide Distribution - US (nationwide) and in Canada, Mexico and Latin America.
Product Description
Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P and 350P device (SAM 300P and 350P). || Automated External Defibrillator electrode supplies. The Pedi-Pak is specifically designed for use with the HeartSine Samaritan PAD 300P and 350P device. It contains defibrillator electrodes in a sealed foil pouch and a battery pack in a sealed plastic housing.
Manufacturer
Heartsine Technologies, Limited
1 Event
- Recall of Device Recall PadPak and PediPak accessories for the HeartSine SamaritanPAD 300P and 350P device

Manufacturer

Heartsine Technologies, Limited

Manufacturer Address
Heartsine Technologies, Limited, 203 Airport Road West, Belfast United Kingdom
Manufacturer Parent Company (2017)
Stryker
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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