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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: OUTSET MEDICAL, INC. TABLO X HEMODIALYSIS SYSTEM DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

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OUTSET MEDICAL, INC. TABLO X HEMODIALYSIS SYSTEM DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM Back to Search Results
Model Number PN-0003000
Device Problems No Display/Image (1183); Failure to Power Up (1476)
Patient Problem Loss of consciousness (2418)
Event Date 09/10/2021
Event Type  Injury  
Event Description
It was reported that a patient with a history of cardiac stenosis coded twice during dialysis treatment on tablo. The care personnel initiated cardiopulmonary resuscitation (cpr), and the patient was revived and was stable. During the second code, the care personnel attempted to return the blood and end the treatment; however, it was reported that the tablo touchscreen froze. The nurse disconnected the patient from the tablo device and there was estimated 240 ml of blood loss. The patient was revived and was stable post-treatment. Based on the available information, it is unknown if the code event was related to the patient¿s underlying condition; therefore, this event is being reported as a serious injury.
 
Manufacturer Narrative
An investigation conducted by outset technical team via log review confirmed that the user manually stopped the blood pump at 66 and half minutes into a two and half-hour treatment. The treatment was ended, which is when the ¿new saline bag required¿ alarm was triggered. By this time, 800 ml of saline was already used by the site and there was not enough saline to return the blood, hence ¿alarm saline bag required¿ was prompted. It was noted that 400 ml of saline was delivered in the six minutes prior to the alarm new saline bag required. The outset technical team concluded that this strongly indicates that the patient was in distress prior to the alarm. It could not be confirmed if the graphic user interface (gui) went black at this point. A field service engineer (fse) replaced the touchscreen on the system. A comprehensive dhr (device history record) review was performed. There were no non-conformances noted upon review of the dhr for the console and it was confirmed that this console met all inspections and test criteria. Prior to final release and distribution to customers, all tablo consoles are inspected, tested and verified through in-process inspection and testing, followed by a quality inspection after manufacturing.
 
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Brand NameTABLO X HEMODIALYSIS SYSTEM
Type of DeviceDIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM
Manufacturer (Section D)
OUTSET MEDICAL, INC.
3052 orchard drive
san jose CA 95134
MDR Report Key12619848
MDR Text Key280806413
Report Number3010355846-2021-00071
Device Sequence Number1
Product Code KDI
Combination Product (y/n)N
PMA/PMN Number
K190793
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,health
Type of Report Initial
Report Date 10/12/2021
1 Device was Involved in the Event
0 Patients were Involved in the Event:
Date FDA Received10/12/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator
Device Model NumberPN-0003000
Device Catalogue NumberPN-0003000
Was Device Available for Evaluation? Yes
Was the Report Sent to FDA?
Distributor Facility Aware Date09/13/2021
Event Location No Information
Date Manufacturer Received09/13/2021
Is This a Reprocessed and Reused Single-Use Device? No

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