FDA Adverse Event Malfunction Summary report: N

KIT GRP A STREP 30 TEST VERITOR

MDR report key: 15953207 · Received December 9, 2022

Report

Report Number
3006948883-2022-00196
Event Type
Malfunction
Date Received
December 9, 2022
Date of Event
November 16, 2022
Report Date
March 7, 2023
Manufacturer
BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.
Product Code
GTY
UDI-DI
00382902560401
PMA / PMN Number
K122718
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 0

H.6 INVESTIGATION SUMMARY THIS STATEMENT IS TO SUMMARIZE THE INVESTIGATION RESULTS REGARDING A COMPLAINT THAT ALLEGES DISCREPANT SPECIMEN STORAGE TIME ON THE PACKAGE INSERT (PI) AND QUICK REFERENCE GUIDE (QRG) WHEN USING BD GRP A STREP 30 TEST VERITOR KIT (MATERIAL # 256040), BATCH NUMBER 1295326. BD QUALITY PERFORMS A SYSTEMATIC APPROACH TO INVESTIGATE LABELLING / PACKAGING ISSUE COMPLAINTS. THIS APPROACH INVOLVES REVIEW OF MANUFACTURING BATCH HISTORY RECORDS, TESTING OF RETENTION SAMPLES, AND TESTING OF CUSTOMER RETURNED SAMPLES, IF APPLICABLE. BASED ON THE PROVIDED INFORMATION, IT WAS UNDERSTOOD THAT THE CUSTOMER REPORTED DIFFERENT SPECIMEN STORAGE TIME STATED ON THE PI AND QRG IN THE KIT AND THEY WANTED TO CONFIRM IF THE SPECIMEN STORAGE WAS 48 HOURS (AS STATED IN PI) OR 72 HOURS (AS STATED IN THE QRG) AS THEY FOUND DISCREPANT INFORMATION FOR THE SAME PRODUCT. BHR REVIEW AND RETAIN SAMPLE ANALYSIS WAS NOT PERFORMED BECAUSE THE REPORTED ISSUE ALLEGING THE DISCREPANT INFORMATION NOT WITH PRODUCT MALFUNCTION. FURTHER INVESTIGATION WAS DONE BY BD RESEARCH & DEVELOPMENT (R & D) ON THIS ISSUE, AND IT WAS CONFIRMED THAT THE INSERT HAS A DIFFERENT TIME SPECIMEN STORAGE OF 48HOURS VS QRG OF 72HOUR. BD WILL UPDATE THE PI TO 72HOURS TO ALIGN WITH THE QRG PER BALTQP2106, LABELING DEVELOPMENT REQUEST (LDR). THE SPECIMEN STORAGE TIME CHANGE TO 48HOURS WAS AN ERROR AND THE PI WILL BE REVERSED TO SAY 72 HOURS. THIS COMPLAINT WAS CONFIRMED. THE ROOT CAUSE WAS TRACED TO LABELLING. CURRENTLY, THERE ARE NO ADVERSE TRENDS IDENTIFIED FOR LABELLING / PACKAGING ISSUE. BD QUALITY WILL CONTINUE TO MONITOR FOR TRENDS.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE CUSTOMER DISCOVERED A DISCREPANCY BETWEEN THE PACKAGE INSERT AND THE QUICK START GUIDE IN THE KIT GRP A STREP 30 TEST VERITOR. THE PACKAGE INSERT STATED THAT SPECIMENS COULD BE STORED FOR 48 HRS HOURS AT 2-8 C, AND THE QUICK START GUIDE INDICATES 72 HOURS AT 2-8 C. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER WANTS TO CONFIRM IF THE SPECIMEN STORAGE WAS 48 HRS (AS STATED IN PI) OR 72 HOURS (AS STATED IN THE QUICK REFERENCE GUIDE) AS THEY FOUND DISCREPANT INFORMATION FOR THE SAME PRODUCT.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE CUSTOMER DISCOVERED A DISCREPANCY BETWEEN THE PACKAGE INSERT AND THE QUICK START GUIDE IN THE KIT GRP A STREP 30 TEST VERITOR. THE PACKAGE INSERT STATED THAT SPECIMENS COULD BE STORED FOR 48 HRS HOURS AT 2-8 C, AND THE QUICK START GUIDE INDICATES 72 HOURS AT 2-8 C. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER WANTS TO CONFIRM IF THE SPECIMEN STORAGE WAS 48 HRS (AS STATED IN PI) OR 72 HOURS (AS STATED IN THE QUICK REFERENCE GUIDE) AS THEY FOUND DISCREPANT INFORMATION FOR THE SAME PRODUCT

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2543056 KIT GRP A STREP 30 TEST VERITOR ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP. GTY BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD. 256040 1295326 00382902560401

Patients

Seq Age Sex Outcome Treatment
1 Unknown