FDA Adverse Event Malfunction Summary report: N

I-STAT 6+ CARTRIDGE

MDR report key: 8631147 · Received May 22, 2019

Report

Report Number
2245578-2019-00130
Event Type
Malfunction
Date Received
May 22, 2019
Date of Event
May 9, 2019
Report Date
July 26, 2019
Manufacturer
ABBOTT POINT OF CARE
Product Code
JGS
UDI-DI
10054749000088
PMA / PMN Number
K912387
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

APOC INCIDENT #: (B)(4). THE INVESTIGATION WAS COMPLETED ON 07/23/2019. A REVIEW OF THE DEVICE HISTORY RECORD (DHR) CONFIRMED THE CARTRIDGE LOT MET FINISHED GOODS (FG) RELEASE CRITERIA. RETAINED TESTING MET THE ACCEPTANCE CRITERIA OUTLINED IN APPENDIX 1 OF Q04.01.003 REV. AD (PRODUCT COMPLAINT LEVEL 2 AND LEVEL 3 INVESTIGATION PROCEDURE). NO DEFICIENCY HAS BEEN DETERMINED FOR 6+ LOT K18301.

Additional Manufacturer Narrative · 1

APOC INCIDENT #: (B)(4). APOC LABELING WILL BE EVALUATED DURING THE INVESTIGATION AS PERTAINING TO THE EVENT.

Description of Event or Problem · 1

ON (B)(6) 2019, ABBOTT POINT OF CARE WAS CONTACTED BY A CUSTOMER REGARDING I-STAT 6+ CARTRIDGES THAT YIELDED A SUSPECTED A DISCREPANT POTASSIUM RESULT ON A PATIENT. THERE WAS NO PATIENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT. METHOD: I-STAT, RESULT: >9, LAB INSTRUMENT : NORMAL (ACTUAL RESULT UNKNOWN). CUSTOMER HAS NOT PROVIDED COLLECT/TEST TIMES, OR PATIENT INFORMATION. THERE ARE NO INJURIES ASSOCIATED WITH THIS EVENT. AT THIS TIME THERE IS NO REASON TO SUSPECT A MALFUNCTION EXISTS. THE REPORTING DECISION WAS BASED ON LIMITED INFORMATION AVAILABLE THAT SUGGESTS THE PRODUCT WAS NOT PERFORMING WITHIN THE VARIABILITY OF THE ASSAY. THE INVESTIGATION IS UNDERWAY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
427401 I-STAT 6+ CARTRIDGE 6+ CARTRIDGE JGS ABBOTT POINT OF CARE NA K18301 10054749000088

Patients

Seq Age Sex Outcome Treatment
1