Heartsine Technologies, Limited: Medical Device Recalls in 2012

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Heartsine Technologies, Limited in 2012. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

2012

2014

HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753; 10C00200000 to 10C00210106 Product Usage: Samaritan 300/300P PAD is indicated for use on victims of sudden cardiac arrest who are exhibiting the following signs: Unconsciousness Not breathing Without circulation