FDA Adverse Event Injury Summary report: N

GLUCOCARD EXPRESSION BLOOD GLUCOSE TEST SYSTEM

MDR report key: 15967562 · Received December 13, 2022

Report

Report Number
9616936-2022-00001
Event Type
Injury
Date Received
December 13, 2022
Date of Event
February 12, 2022
Report Date
December 10, 2022
Manufacturer
APEX BIOTECHNOLOGY CORP.
Product Code
NBW
UDI-DI
00015482570057
PMA / PMN Number
K113098
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

INFORMATION PROVIDED BY IMPORTER (ARKRAY FACTORY USA, INC.): COMPLAINED PRODUCTS WERE NOT RETURNED FOR EVALUATION. RETAIN STRIPS OF SPECIFICED LOT WERE TESTED WITH REFERENCE METER AND PASSED TESTING WITH NO FAILURES DETECTED. IF EITHER METER OR STRIPS IS RETURNED, ARKRAY (THE IMPORTER) WILL EVALUATE THE PRODUCT AND FILE A FOLLOW-UP REPORT. MANUFACTURER NARRATIVE: 1. IN-HOUSE CLINICAL CAPILLARY BLOOD TEST (FINGER TIP BLOOD TEST), VENOUS BLOOD TEST AND CONTROL SOLUTION TEST FOR RETAIN METER AND THE SAME LOT OF RETAIN STRIPS ARE CONDUCTED. THE RESULTS ARE PASSED WITH SPECIFIED SPECIFICATIONS. PLEASE REFER TO THE ATTACHMENT "22000072-S8 FINGER TIP TEST RESULT", ATTACHMENT "22000072-S8 VENOUS BLOOD TEST RESULT" AND ATTACHMENT "22000072-S8 CONTROL SOLUTION TEST RESULT" FOR DETAILS. 2. ROOT CAUSE OR POSSIBLE REASON FOR THIS COMPLAINT HAS NOT BEEN IDENTIFIED. 3. IF THE COMPLAINED METER OR STRIPS RETURNED FROM THE USER THROUGH THE IMPORTER, WE, APEX BIOTECHNOLOGY CORP. (THE MANUFACTURER) WILL EVALUATE THE PRODUCT AND FILE A FOLLOW-UP REPORT.

Additional Manufacturer Narrative · 0

INFORMATION PROVIDED BY IMPORTER (ARKRAY FACTORY USA, INC.) (UPDATED): ON 02 DEC 2022, METER AND ELEVEN STRIPS OF SPECIFIED LOT WERE RETURNED FOR INVESTIGATION. RETURNED STRIPS WERE TESTED ALONG WITH RETAIN STRIPS WITH RETURNED METER. METER AND STRIPS PASSED TESTING WITH NO FAILURES DETECTED. METER WILL BE RETURNED TO THE MANUFACTURER FOR FURTHER INVESTIGATION. MANUFACTURER NARRATIVE (UPDATED): 1. THE COMPLAINED METER AND EMPTY TEST STRIP BOTTLE OF SPECIFIED LOT WERE RECEIVED ON 19 DEC 2022. 2. INVESTIGATION RESULTS OF THE RETURNED METER, INCLUDING FUNCTIONAL TEST, ARE NORMAL. PLEASE REFER TO ATTACHMENT 1 FOR DETAILS. 3. IN-HOUSE CLINICAL CAPILLARY BLOOD TEST (FINGER TIP BLOOD TEST) FOR THE RETURNED METER WITH SPECIFIED LOT OF RETAIN TEST STRIPS IS CONDUCTED. THE RESULTS ARE PASSED WITHIN THE SPECIFICATION. PLEASE REFER TO ATTACHMENT 3 FOR DETAILS. (AMENDMENT FOR THE "22000072-S8 FINGER TIP RESULT" OF THE FIRST EMDR SUBMISSION ON 13 DEC 2022: TO REMOVE INFORMATION NOT RELATED. PLEASE SEE ATTACHMENT 2.) 4. ADDITIONAL MOISTURE TEST TO THE DESICCANT IN RETURNED TEST STRIP BOTTLE IS PERFORMED AND THE RESULT IS ACCEPTABLE. PLEASE REFER TO ATTACHMENT 4 FOR DETAILS. 5. ROOT CAUSE OR POSSIBLE REASON FOR THIS COMPLAINT HAS NOT BEEN IDENTIFIED.

Description of Event or Problem · 0

THE CALLER INDICATED THE GLUCOCARD EXPRESSION METER WAS READING HIGH. THE CALLER PERFORMED A CONTROL SOLUTION TEST WITH A RESULT OF 117, WITH A RANGE OF 97-117. THEN THE CALLER FOUND THIS CONTROL SOLUTION TO BE FOR A RELION PREMIER METER (CSTN04CN), WHICH IS THE INCORRECT CONTROL SOLUTION FOR GLUCOCARD EXPRESSION METER. THE CALLER PERFORMED BACK-TO-BACK BLOOD TESTS WITH RESULTS OF 108 AND 110. IMPORTER EXPLAINED 20% VARIANCE. THE CUSTOMER STATED THAT LAST NIGHT AT 3:30 AM THEY WERE FEELING BAD. CUSTOMER STATED THEY WERE FEELING DISORIENTED AND TESTED THEIR BLOOD SUGAR WITH A RESULT OF 75. THE CUSTOMER CALLED THE PARAMEDICS WHO ARRIVED AND TESTED THEIR BLOOD GIVING THEM A READING OF 35. THE PARAMEDICS ADVISED THAT THEY EAT FOOD TO INCREASE THEIR BLOOD SUGAR, SO THEY ATE A PEANUT BUTTER SANDWICH AND DRANK A SODA. THE CUSTOMER TOLD IMPORTER THAT THE REASON THEY CALLED THE PARAMEDICS WAS DIRECTLY DUE TO THE READINGS OF THE METER. IMPORTER EXPLAINED THAT THEY WOULD SEND A REPLACEMENT METER AND TEST STRIPS AND THEY WOULD ARRIVE IN 3-5 BUSINESS DAYS WITH A RETURN LABEL TO SEND BACK THE COMPLAINT PRODUCTS.

Description of Event or Problem · 0

THE CALLER INDICATED THE GLUCOCARD EXPRESSION METER WAS READING HIGH. THE CALLER PERFORMED A CONTROL SOLUTION TEST WITH A RESULT OF 117, WITH A RANGE OF 97-117. THEN THE CALLER FOUND THIS CONTROL SOLUTION TO BE FOR A RELION PREMIER METER (CSTN04CN), WHICH IS THE INCORRECT CONTROL SOLUTION FOR GLUCOCARD EXPRESSION METER. THE CALLER PERFORMED BACK-TO-BACK BLOOD TESTS WITH RESULTS OF 108 AND 110. IMPORTER EXPLAINED 20% VARIANCE. THE CUSTOMER STATED THAT LAST NIGHT AT 3:30 AM THEY WERE FEELING BAD. CUSTOMER STATED THEY WERE FEELING DISORIENTED AND TESTED THEIR BLOOD SUGAR WITH A RESULT OF 75. THE CUSTOMER CALLED THE PARAMEDICS WHO ARRIVED AND TESTED THEIR BLOOD GIVING THEM A READING OF 35. THE PARAMEDICS ADVISED THAT THEY EAT FOOD TO INCREASE THEIR BLOOD SUGAR, SO THEY ATE A PEANUT BUTTER SANDWICH AND DRANK A SODA. THE CUSTOMER TOLD IMPORTER THAT THE REASON THEY CALLED THE PARAMEDICS WAS DIRECTLY DUE TO THE READINGS OF THE METER. IMPORTER EXPLAINED THAT THEY WOULD SEND A REPLACEMENT METER AND TEST STRIPS AND THEY WOULD ARRIVE IN 3-5 BUSINESS DAYS WITH A RETURN LABEL TO SEND BACK THE COMPLAINT PRODUCTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
424570 GLUCOCARD EXPRESSION BLOOD GLUCOSE TEST SYSTEM GLUCOCARD EXPRESSION NBW APEX BIOTECHNOLOGY CORP. 571100 B4S2201018 00015482570057

Patients

Seq Age Sex Outcome Treatment
1 74 YR Male Required Intervention| L