FDA Adverse Event Malfunction Summary report: N

I-STAT TROPONIN (CTNI) CARTRIDGE

MDR report key: 4100150 · Received September 18, 2014

Report

Report Number
2245578-2014-00057
Event Type
Malfunction
Date Received
September 18, 2014
Date of Event
July 31, 2014
Report Date
August 20, 2014
Manufacturer
ABBOTT POINT OF CARE
Product Code
MMI
PMA / PMN Number
K031739
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE INVESTIGATION WAS COMPLETED ON 10/10/2014. THE CUSTOMER DID NOT RETURN PRODUCT FOR INVESTIGATION. RETAIN CARTRIDGES WERE TESTED AND ARE FUNCTIONING ACCORDING TO SPECIFICATION.

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

ON (B)(6) 2014, ABBOTT POINT OF CARE WAS CONTACTED BY A CUSTOMER REGARDING I-STAT TROPONIN CARTRIDGES THAT YIELDED A SUSPECTED DISCREPANT RESULT OF 0.31 ON A FEMALE PATIENT. THERE WAS NO ADDITIONAL PATIENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT. DATE: (B)(6) 2014, TIME: 0041, INSTRUMENT: I-STAT, CTNI: 0.31, SAMPLE: A; 0055, I-STAT, 0.00, B. THERE WERE NO INJURIES REPORTED WITH THIS EVENT. THE INVESTIGATION IS UNDERWAY.

Description of Event or Problem · 1

N/A

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
578644 I-STAT TROPONIN (CTNI) CARTRIDGE CTNI CARTRIDGE MMI ABBOTT POINT OF CARE NA P14126

Patients

Seq Age Sex Outcome Treatment
1