FDA Adverse Event Malfunction Summary report: N

BD POSIFLUSH¿ SYRINGE

MDR report key: 8432310 · Received March 19, 2019

Report

Report Number
1911916-2019-00282
Event Type
Malfunction
Date Received
March 19, 2019
Date of Event
March 5, 2019
Report Date
March 11, 2019
Manufacturer
BD MEDICAL (BD WEST) MEDICAL SURGICAL
Product Code
NGT
PMA / PMN Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(6). INVESTIGATION SUMMARY: SINCE NO SAMPLES DISPLAYING THE CONDITION REPORTED ARE AVAILABLE FOR EXAMINATION, WE WERE UNABLE TO FULLY INVESTIGATE THIS INCIDENT. NO ROOT CAUSE CAN BE DETERMINED AS NO SAMPLES WERE RECEIVED. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. INFORMATION WILL BE CAPTURED ON TREND REPORTS AND MONITORED MONTHLY. OUR BUSINESS TEAM REGULARLY REVIEWS THE COLLECTED DATA FOR IDENTIFICATION OF EMERGING TRENDS. BASED ON NO SAMPLE, THE INVESTIGATION CONCLUDED, BD WAS NOT ABLE TO VERIFY THE INDICATED FAILURE. A DEVICE HISTORY RECORD REVIEW WAS COMPLETED WITH ZERO DEFECTS FOUND. NO QUALITY NOTIFICATIONS WERE WRITTEN FOR THIS BATCH, NOR FOR THE ASSOCIATED ASSEMBLY BATCHES. INVESTIGATION CONCLUSION: THIS IS THE 1ST COMPLAINT FOR LOT # 8082847 FOR THIS TYPE OF DEFECT OR SYMPTOM. THERE WAS NO DOCUMENTATION FOR THIS TYPE OF DEFECT DURING THE ENTIRE PRODUCTION RUN OF THIS BATCH. ROOT CAUSE DESCRIPTION: UNDETERMINED.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING USE OF BD POSIFLUSH¿ SYRINGE BARREL/FLANGE WAS BROKEN. DISCONTINUED USE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
228128 BD POSIFLUSH¿ SYRINGE PRE-FILLED SYRINGE NGT BD MEDICAL (BD WEST) MEDICAL SURGICAL 8082847

Patients

Seq Age Sex Outcome Treatment
1 Other