FDA Adverse Event Malfunction Summary report: N

I-STAT CHEM 8+ CARTRIDGE

MDR report key: 6939418 · Received October 10, 2017

Report

Report Number
2245578-2017-00485
Event Type
Malfunction
Date Received
October 10, 2017
Date of Event
August 9, 2016
Report Date
October 10, 2017
Manufacturer
ABBOTT POINT OF CARE
Product Code
JGS
UDI-DI
10054749001917
PMA / PMN Number
K053110
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). APOC LABELING WAS EVALUATED DURING THE INVESTIGATION AS PERTAINING TO THE EVENT. THE INVESTIGATION WAS COMPLETED ON (B)(6) 2016. RETAIN PRODUCT WAS TESTED AND FUNCTIONING ACCORDING TO SPECIFICATION. RETURN PRODUCT WAS NOT AVAILABLE FOR INVESTIGATION. INVESTIGATION: A REVIEW OF THE DEVICE HISTORY RECORD (DHR) CONFIRMED THAT THE CARTRIDGE LOT MET FINISHED GOODS (FG) RELEASE CRITERIA. RETAINED CARTRIDGES FROM THE LOT WERE TESTED USING WHOLE BLOOD (WB) AND I-STAT LEVEL 2 CONTROL (L2). TESTING MET THE ACCEPTANCE CRITERIA FOUND IN (B)(4) - PRODUCT COMPLAINT LEVEL 2 AND LEVEL 3 INVESTIGATION PROCEDURE. . THE CUSTOMER COMPLAINT WAS NOT REPRODUCED. ASSESSMENT: THE COMPLAINT INVESTIGATION CONCLUDED THERE WAS NO PRODUCT DEFICIENCY AND THAT THE I-STAT CARTRIDGE LOT IS MEETING SPECIFICATION. NO REPEATS ON THE I-STAT OR LABORATORY. TWO DIFFERENT SAMPLES WERE TESTED.

Description of Event or Problem · 1

ON (B)(6) 2016, ABBOTT POINT OF CARE WAS CONTACTED BY A CUSTOMER REGARDING I-STAT CHEM8+ CARTRIDGES THAT YIELDED SUSPECTED DISCREPANT SODIUM (NA), CHLORIDE (CL), AND POTASSIUM (K) RESULT ON A PATIENT. THERE WERE NO INJURIES ASSOCIATED WITH THIS EVENT. THERE WAS NO ADDITIONAL PATIENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT. THERE WAS NO REPEAT ON I-STAT. RETURN PRODUCT IS NOT AVAILABLE FOR INVESTIGATION. METHOD , DATE , TEST TIME, NA (MMOL) , CL (MMOL) , K(MMOL) : I-STAT , (B)(6) 2016, 17:13 , 111 , >140 , 3.3 ; BECKMAN , (B)(6) 2016 , 17:13 , 139 , 100 , 4.1 . AT THE TIME OF THE EVENT THERE WAS NO INDICATION OF A PRODUCT MALFUNCTION BASED ON THE INFORMATION PROVIDED AND ASSESSED BY APOC, HOWEVER THIS MDR IS A RETROSPECTIVE FILING IN RESPONSE TO AN OBSERVATION FROM AN FDA INSPECTION CONDUCTED(B)(6) 2017 AT ABBOTT POINT OF CARE ((B)(4)).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
718851 I-STAT CHEM 8+ CARTRIDGE CHEM 8+ CARTRIDGE JGS ABBOTT POINT OF CARE NA H16132 10054749001917

Patients

Seq Age Sex Outcome Treatment
1