Sorin Group Italia SRL - CRF recalls

Sorin Group Italia SRL - CRF has 9 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 4 Oct 2017.

Total recalls9since 2017

Last 12 months0reported

Class I00% of total

Ongoing0latest 4 Oct 2017

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 9 100%Class III 0 0%

Why sorin group italia srl - crf is recalled

Other Reasons667%
Device Malfunction333%

Product types

Pacemakers & Defibrillators667%
Other Medical Devices333%

By year

20179100%

All sorin group italia srl - crf recalls, newest first

9 total

Reported	Class	Recall	Company	Reason	Where
4 Oct 2017Device	CLASS II	Platinium DR recalled by Sorin Group Italia SRL - CRF	Sorin Group Italia SRL - CRF	Other	Nationwide
4 Oct 2017Device	CLASS II	Platinium CRT DF1 recalled by Sorin Group Italia SRL - CRF	Sorin Group Italia SRL - CRF	Other	Nationwide
4 Oct 2017Device	CLASS II	Platinium VR recalled by Sorin Group Italia SRL - CRF	Sorin Group Italia SRL - CRF	Other	Nationwide
4 Oct 2017Device	CLASS II	Platinium DR DF4 recalled by Sorin Group Italia SRL - CRF	Sorin Group Italia SRL - CRF	Other	Nationwide
4 Oct 2017Device	CLASS II	Platinium Crt-d recalled by Sorin Group Italia SRL - CRF	Sorin Group Italia SRL - CRF	Other	Nationwide
4 Oct 2017Device	CLASS II	Platinium VR DF4 recalled by Sorin Group Italia SRL - CRF	Sorin Group Italia SRL - CRF	Other	Nationwide
24 May 2017Device	CLASS II	Paradym Models: VR 8250, DR 8550, Crt-d 8750, RF VR 9250, RF DR recalled	Sorin Group Italia SRL - CRF	Device Malfunction	Nationwide
24 May 2017Device	CLASS II	Intensia Models: VR 124, DR 154, Crt-d 174 Product Usage: Ovatio VR recalled	Sorin Group Italia SRL - CRF	Device Malfunction	Nationwide
24 May 2017Device	CLASS II	Ovatio Models: VR 6250, DR 6550, CRT 6750. Product Usage: Ovatio VR recalled	Sorin Group Italia SRL - CRF	Device Malfunction	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.