FDA recall Z-1119-2020

LivaNova USA Inc. · Class III · device

Product

LivaNova Sorin Connect DPIII KOMPL. S5 REF 96-415-130, 2017-08-15, IPX1, RXOnly, (01)04033817901594 Product Usage: The S5 System is used to perform, control and monitor extracorporeal blood circulation during an operation for up to six hours.

Reason for recall

Incorrect labeling; it was identified that some Datapad devices contained incorrect labels. Specifically the manufacturing date in the production identifier was incorrect and the manufacturing date on the unique device identifier label was labeled in the format of yy-mm-dd instead of yyyy-mm-dd.

Distribution

US: NJ and CA

Key facts

Status
Terminated
Initiation date
2019-01-28
Report date
2020-02-19
Termination date
2022-01-31
Voluntary/Mandated
Voluntary: Firm initiated
Location
Arvada, CO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1119-2020