Sorin Group Deutschl recalls

Sorin Group Deutschl has 4 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 31 Jan 2018. The most frequent reason is device malfunction.

Total recalls4since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 31 Jan 2018

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 0 0%Class II 4 100%Class III 0 0%

Why sorin group deutschl is recalled

Device Malfunction4100%

Product types

Other Medical Devices4100%

By year

2018125%
2014250%
2013125%

All sorin group deutschl recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
31 Jan 2018Device	CLASS II	CP5 Centrifugal Pump, made up of the drive unit recalled	Sorin Group Deutschl	Device Malfunction	N/A
5 Feb 2014Device	CLASS II	CP5 centrifugal pump system recalled by Sorin Group Deutschland	Sorin Group Deutschl	Device Malfunction	Nationwide
5 Feb 2014Device	CLASS II	S5/C5 Heart-lung machine recalled by Sorin Group Deutschland	Sorin Group Deutschl	Device Malfunction	Nationwide
13 Nov 2013Device	CLASS II	S5 Heart-lung machine, Stockert S5 System recalled	Sorin Group Deutschl	Device Malfunction	14 states

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.