Epoxy used during manufacturing of the LifeSPARC Pump may have uncured epoxy. if undetectable curing may result in added risk of early pump failure,
Cardiac Assist
A software update (v1.1.5) has been developed to address the issue of Critical Failure which can occur on the LifeSPARC Controller. The Critical Failure was first addressed in the firm's recall initiated July 21, 2022. During the Critical Failure, the software freezes or crashes and the screen does not display data.
Critical Failure of the LifeSPARC controller when the software freezes or crashes and the screen does not display data.
Top label of the outer package of the collection kit Item 5820-3118 showed expiration date of 2022/05/01 (correct expiration date) while side label showed expiration date of 2021/05/01 (incorrect expiration date)
On 02/26/2021, it was found that there were incorrectly packaged Dilator sets in Finished Goods. On 03/1/2021, it was confirmed that 14 kits containing the impacted products had been distributed to the field.
Failure to prime due to an assembly error
Failure to prime due to an assembly error
Failure to prime due to an assembly error
Failure to prime due to an assembly error
Failure to prime due to an assembly error
Failure to prime due to an assembly error
Failure to prime due to an assembly error
Failure to prime due to an assembly error
The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo Venous cannula.