FDA Adverse Event Malfunction Summary report: N

BD PRESET¿ ARTERIAL BLOOD COLLECTION SYRINGE

MDR report key: 17024644 · Received May 30, 2023

Report

Report Number
9617032-2023-00623
Event Type
Malfunction
Date Received
May 30, 2023
Date of Event
April 12, 2023
Report Date
May 24, 2023
Manufacturer
BECTON, DICKINSON AND COMPANY (BD)
Product Code
JKA
PMA / PMN Number
K022426
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION SUMMARY: MATERIAL #: 364314. LOT/BATCH #: 2091547. BD HAD NOT RECEIVED SAMPLES OR PHOTOS FOR INVESTIGATION. THEREFORE, 10 RETENTION SAMPLES FROM BD INVENTORY WERE EVALUATED BY VISUAL EXAMINATION AND NO ISSUES WERE OBSERVED RELATING TO DEFECTIVE SCALE MARKINGS AS ALL SAMPLES MET SPECIFICATIONS. BASED ON A REVIEW OF THE DEVICE HISTORY RECORD FOR THE INCIDENT LOT, ALL PRODUCT SPECIFICATIONS AND REQUIREMENTS FOR LOT RELEASE WERE MET. THERE WERE NO RELATED QUALITY ISSUES DURING MANUFACTURING OF THE PRODUCT. THIS COMPLAINT IS UNABLE TO BE CONFIRMED FOR THE INDICATED FAILURE MODE DEFECTIVE SCALE MARKINGS. BD WAS NOT ABLE TO IDENTIFY A ROOT CAUSE FOR THE INDICATED FAILURE MODE. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. OUR BUSINESS TEAM REGULARLY REVIEWS THE COLLECTED DATA FOR IDENTIFICATION OF EMERGING TRENDS.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHILE USING THE BD PRESET¿ ARTERIAL BLOOD COLLECTION SYRINGE THAT THE SCALE OF ABG IS NOT CLEAR. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER THE SCALE OF ABG IS NOT CLEAR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1885739 BD PRESET¿ ARTERIAL BLOOD COLLECTION SYRINGE BLOOD SPECIMEN COLLECTION DEVICE JKA BECTON, DICKINSON AND COMPANY (BD) 2091547

Patients

Seq Age Sex Outcome Treatment
1 Unknown