FDA Adverse Event Malfunction Summary report: N

BD POSIFLUSH¿ PRE-FILLED SALINE SYRINGE

MDR report key: 15242159 · Received August 17, 2022

Report

Report Number
1710034-2022-00437
Event Type
Malfunction
Date Received
August 17, 2022
Date of Event
July 12, 2022
Report Date
August 5, 2022
Manufacturer
BD MEDICAL (BD WEST) MEDICAL SURGICAL
Product Code
NGT
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION SUMMARY: A DEVICE HISTORY RECORD REVIEW WAS COMPLETED BY OUR QUALITY ENGINEER TEAM FOR PROVIDED MATERIAL NUMBER: 306594 AND LOT NUMBER: 1152092. THE REVIEW DID NOT REVEAL ANY DETECTED ABNORMALITIES DURING THE PRODUCTION PROCESS THAT COULD HAVE CONTRIBUTED TO THIS DEFECT AND ALL QUALITY TESTS WERE FOUND TO BE WITHIN SPECIFICATION. AS A SAMPLE WAS UNAVAILABLE FOR RETURN, A THOROUGH SAMPLE INVESTIGATION COULD NOT BE COMPLETED. BASED ON THE INVESTIGATION RESULTS, AN EXACT CAUSE FOR THIS INCIDENT COULD NOT BE IDENTIFIED. THERE ARE QUALITY CONTROLS CURRENTLY IN PLACE TO DETECT THIS TYPE OF DEFECT DURING THE PRODUCTION PROCESS. FURTHER ACTION HAS NOT BEEN DETERMINED NECESSARY AT THIS TIME. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. OUR QUALITY TEAM REGULARLY REVIEWS THE COLLECTED DATA FOR IDENTIFICATION OF EMERGING TRENDS.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE PLUNGER ROD BROKE ON THE BD POSIFLUSH¿ PRE-FILLED SALINE SYRINGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: (B)(6) 2022 WHEN THE NURSE OPENED THE NEWLY PACKAGED FLUSH IN THE TREATMENT ROOM OF THE FOURTH AREA, SHE FOUND THAT THE TUBE HANDLE WAS BROKEN AND COULD NOT USE THE FLUSH NORMALLY, AND IMMEDIATELY REPLACED IT WITH A NEW ONE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2013659 BD POSIFLUSH¿ PRE-FILLED SALINE SYRINGE SALINE VASCULAR ACCESS FLUSH NGT BD MEDICAL (BD WEST) MEDICAL SURGICAL 1152092

Patients

Seq Age Sex Outcome Treatment
1 Unknown