Sorin Group Italia SRL: 8 recalls on record

Recalls filed with 1 agency: FDA (8).

First recall on record: January 29, 2014. Most recent: September 30, 2020.

Risk classification: Class II: 8

Most recent recalls

DateAgencyProduct
September 30, 2020FDAPerceval Single Use Accessory Kit, Size S, REF: ICV1349, Sterile EO, Rx Only, CE, UDI: 80…Z-2986-2020
September 30, 2020FDAPerceval Single Use Accessory Kit, Size M, REF: ICV1346, Sterile EO, Rx Only, CE, UDI: 80…Z-2985-2020
October 4, 2017FDAPlatinium CRT-D 1741, Model Number TDF037U, UDI/GTIN 08031527015484, Implantable cardiove…Z-3233-2017
October 4, 2017FDAPlatinium VR DF4 1240, Model Number TDF035U, UDI/GTIN 08031527015460, Implantable cardiov…Z-3231-2017
October 4, 2017FDAPlatinium DR DF4 1540, Model Number TDF036U, UDI/GTIN 08031527015477, Implantable cardiov…Z-3232-2017
May 24, 2017FDAINTENSIA Models: VR 124, DR 154, CRT-D 174 Product Usage: OVATIO VR 6250, OVATIO DR …Z-2114-2017
May 24, 2017FDAOVATIO Models: VR 6250, DR 6550, CRT 6750. Product Usage: OVATIO VR 6250, OVATIO DR…Z-2112-2017
January 29, 2014FDAORCHESTRA/ORCHESTRA PLUS ProgrammerZ-0805-2014

Questions about this company

How many recalls does Sorin Group Italia SRL have?
Recalert has 8 U.S. recalls on record for Sorin Group Italia SRL, published between January 29, 2014 and September 30, 2020.
What was the most recent Sorin Group Italia SRL recall?
FDA recall Z-2986-2020, published September 30, 2020: Perceval Single Use Accessory Kit, Size S, REF: ICV1349, Sterile EO, Rx Only, CE, UDI: 8022057015211 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used t…
Which agencies have handled Sorin Group Italia SRL recalls?
Sorin Group Italia SRL appears as the recalling firm in recalls from: FDA (8).

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