8110 ALARIS SYRINGE PUMP

PUMP, INFUSION

This device is manufactured by CAREFUSION, nan.

The following problems were reported about this device:

Year	Description	Events/year	Type
2021	Naturally Worn	2	Device
2021	Insufficient Information	1	Device
2021	Failure to Calibrate	12	Device
2021	Failure to Analyze Signal	2	Device
2021	Failure to Align	137	Device
2021	Display Difficult to Read	20	Device
2021	Device Sensing Problem	16	Device
2021	Crack	15	Device
2021	Corroded	6	Device
2021	Contamination	131	Device
2021	Communication or Transmission Problem	3	Device
2021	Circuit Failure	3	Device
2021	Break	14	Device
2020	Thermal Decomposition of Device	1	Device
2020	Physical Resistance/Sticking	4	Device
2020	Output Problem	7	Device
2020	No Apparent Adverse Event	1	Device
2020	Naturally Worn	36	Device
2020	Mechanics Altered	1	Device
2020	Failure to Calibrate	11	Device
2020	Failure to Analyze Signal	2	Device
2020	Failure to Align	70	Device
2020	Display Difficult to Read	70	Device
2020	Device Sensing Problem	16	Device
2020	Device Alarm System	1	Device
2020	Deformation Due to Compressive Stress	2	Device
2020	Crack	82	Device
2020	Corroded	99	Device
2020	Contamination	53	Device
2020	Communication or Transmission Problem	2	Device
2020	Circuit Failure	4	Device
2020	Break	98	Device
2020	Application Program Problem	1	Device
2019	Low Blood Pressure/ Hypotension	1	Patient
2019	Thermal Decomposition of Device	1	Device
2019	Pressure Problem	1	Device
2019	Physical Resistance/Sticking	1	Device
2019	Peeled/Delaminated	1	Device
2019	Output Problem	50	Device
2019	No Apparent Adverse Event	2	Device
2019	Naturally Worn	29	Device
2019	Misassembled	1	Device
2019	Inadequate User Interface	1	Device
2019	Inadequacy of Device Shape and/or Size	1	Device
2019	Failure to Calibrate	19	Device
2019	Failure to Analyze Signal	19	Device
2019	Failure to Align	2	Device
2019	Device Sensing Problem	11	Device
2019	Crack	61	Device
2019	Corroded	49	Device
2019	Contamination	17	Device
2019	Circuit Failure	1	Device
2019	Break	68	Device
2019	Application Program Problem	1	Device
2019	Application Program Freezes, Becomes Nonfunctional	7	Device
2018	Insufficient Information	1	Patient
2018	Physical Resistance/Sticking	6	Device
2018	Output Problem	22	Device
2018	No Apparent Adverse Event	1	Device
2018	Naturally Worn	20	Device
2018	Insufficient Information	1	Device
2018	Failure to Calibrate	2	Device
2018	Failure to Analyze Signal	2	Device
2018	Failure to Align	2	Device
2018	Electrical /Electronic Property Problem	1	Device
2018	Device Sensing Problem	3	Device
2018	Crack	30	Device
2018	Corroded	31	Device
2018	Contamination	2	Device
2018	Circuit Failure	1	Device
2018	Break	25	Device
2018	Application Program Freezes, Becomes Nonfunctional	17	Device