FDA Adverse Event Malfunction Summary report: N

I-STAT PT/INR CARTRIDGE

MDR report key: 9480366 · Received December 17, 2019

Report

Report Number
2245578-2019-00300
Event Type
Malfunction
Date Received
December 17, 2019
Date of Event
November 26, 2019
Report Date
March 31, 2020
Manufacturer
ABBOTT POINT OF CARE
Product Code
GJS
UDI-DI
10054749000170
PMA / PMN Number
K020355
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

APOC INCIDENT # (B)(4) . THE INVESTIGATION WAS COMPLETED ON 03/25/2020. A REVIEW OF THE DEVICE HISTORY RECORD (DHR) CONFIRMED THAT THE CARTRIDGE LOT PASSED RELEASE SPECIFICATIONS. RETAINED CARTRIDGE TESTING MET THE ACCEPTANCE CRITERIA OUTLINED IN APPENDIX 1 OF Q04.01.003 REV. AE (PRODUCT COMPLAINT LEVEL 2 AND LEVEL 3 INVESTIGATION PROCEDURE). NO DEFICIENCY HAS BEEN IDENTIFIED.

Description of Event or Problem · 0

NA.

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 PT/INR CARTRIDGES THAT YIELDED A SUSPECTED DISCREPANT PT/INR RESULT IN AN (B)(6) YEAR OLD MALE WITH CHEST PAIN AND SEIZURES. THERE WAS NO ADDITIONAL PATIENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT. METHOD: I-STAT, DATE: 11/26/2019, TIME: 22:23, PT/INR: 55.9 / 5.0. LAB, 11/28/2019, 22:30, 28.1 / 2.81. 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
1278076 I-STAT PT/INR CARTRIDGE PT/INR CARTRIDGE GJS ABBOTT POINT OF CARE NA S19183 10054749000170

Patients

Seq Age Sex Outcome Treatment
1 87 YR