FDA Adverse Event Malfunction Summary report: N

10 ML BD POSIFLUSH SP PRE-FILLED FLUSH SYRINGE NACL 0.9%

MDR report key: 11382689 · Received February 25, 2021

Report

Report Number
1911916-2021-00165
Event Type
Malfunction
Date Received
February 25, 2021
Date of Event
January 12, 2021
Report Date
February 19, 2021
Manufacturer
BD MEDICAL (BD WEST) MEDICAL SURGICAL
Product Code
NGT
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

INITIAL REPORTER FACILITY NAME: (B)(6). INVESTIGATION SUMMARY: A DEVICE HISTORY RECORD REVIEW WAS COMPLETED BY OUR QUALITY ENGINEER TEAM FOR PROVIDED MATERIAL NUMBER 306575 AND LOT NUMBER 0230783. 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. INVESTIGATION CONCLUSION: BASED ON THE INVESTIGATION AND WITH NO SAMPLE ANALYSIS THE SYMPTOM REPORTED BY THE CUSTOMER COULD NOT BE CONFIRMED. WE WILL CONTINUE MONITORING THE COMPLAINT TREND FOR THIS PRODUCT AND SYMPTOM. WITH NO SAMPLE ANALYSIS A PROBABLE ROOT CAUSE COULD NOT BE OFFERED. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT 3 10 ML BD POSIFLUSH¿ SP PRE-FILLED FLUSH SYRINGES NACL 0.9% EXPERIENCED DIFFICULT PLUNGER MOVEMENT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 306575, BATCH NO: 0230783.  HAD USED 3 POSIFLUSH SYRINGES TO FLUSH PATIENT'S CENTRAL LINES AND NOTICED SOME DIFFICULTY WITH THE FLUSH HALF WAY AS IT WAS HARD TO PUSH THE REST OF THE NORMAL SALINE INTO THE CATHETER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
279052 10 ML BD POSIFLUSH SP PRE-FILLED FLUSH SYRINGE NACL 0.9% PREFILLED SALINE SYRINGE NGT BD MEDICAL (BD WEST) MEDICAL SURGICAL 0230783

Patients

Seq Age Sex Outcome Treatment
1