Heart Sync recalls

Heart Sync has 7 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 31 Dec 2014. The most frequent reason is device malfunction.

Total recalls7since 2013

Last 12 months0reported

Class I571% of total

Ongoing0latest 31 Dec 2014

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 5 71%Class II 2 29%Class III 0 0%

Why heart sync is recalled

Device Malfunction571%
Other Reasons229%

Product types

Patient Monitors571%
Pacemakers & Defibrillators229%

By year

2014571%
2013229%

All heart sync recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
31 Dec 2014Device	CLASS I	Adult/Child Radiotransparent Electrode recalled by Heart Sync	Heart Sync	Device Malfunction	Nationwide
31 Dec 2014Device	CLASS I	Adult Radiotranslucent Electrode recalled by Heart Sync	Heart Sync	Device Malfunction	Nationwide
31 Dec 2014Device	CLASS I	Adult/Child Radiotranslucent Electrode recalled by Heart Sync	Heart Sync	Device Malfunction	Nationwide
31 Dec 2014Device	CLASS I	Adult Radiotransparent Electrode recalled by Heart Sync	Heart Sync	Device Malfunction	Nationwide
31 Dec 2014Device	CLASS I	Adult Radiotranslucent Electrode recalled by Heart Sync	Heart Sync	Device Malfunction	Nationwide
5 Jun 2013Device	CLASS II	Vermed, Inc Radiotransparent Defibrillation Electrodes recalled	Heart Sync	Other	Nationwide
5 Jun 2013Device	CLASS II	C100-Physio Radiotransparent Defibrillation Electrodes recalled	Heart Sync	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.