FDA Adverse Event Malfunction Summary report: N

I-STAT CG8+ CARTRIDGE

MDR report key: 13481638 · Received February 8, 2022

Report

Report Number
2245578-2022-00025
Event Type
Malfunction
Date Received
February 8, 2022
Date of Event
January 17, 2022
Report Date
March 16, 2022
Manufacturer
ABBOTT POINT OF CARE
Product Code
CHL
UDI-DI
10054749000163
PMA / PMN Number
K940918
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

APOC INCIDENT: # (B)(4). THE INVESTIGATION WAS COMPLETED ON 09-MAR-2022. THROUGH INVESTIGATION OF A PREVIOUS CUSTOMER COMPLAINT (INCIDENT: (B)(4)), A DEFICIENCY FOR ELEVATED RATE OF UNEXPECTED (HIGH) ICA RESULTS WHEN TESTING WITH CARTRIDGES FROM CG8+ LOT W21198 WAS IDENTIFIED. THIS ISSUE IS UNDER INVESTIGATION UNDER QUALITY RECORDS (QRS) 775835 AND 796335.

Additional Manufacturer Narrative · 0

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

Description of Event or Problem · 0

ON 02-FEB-2022, ABBOTT POINT OF CARE WAS CONTACTED BY A CUSTOMER REGARDING I-STAT CG8+ CARTRIDGES THAT YIELDED A SUSPECTED DISCREPANT IONIZED CALCIUM RESULT OF 2.07 ON A PATIENT. THERE WAS NO ADDITIONAL PATIENT INFORMATION. METHOD, DATE, TESTED RESULT, SAMPLE; I-STAT, (B)(6) 2022, 17:17, 2.07 MMOLL WB; LAB, (B)(6) 2022, NI , 1.39 MMOL/L WB; 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
705691 I-STAT CG8+ CARTRIDGE CG8+ CARTRIDGE CHL ABBOTT POINT OF CARE NA W21198 10054749000163

Patients

Seq Age Sex Outcome Treatment
1 Unknown