FDA Adverse Event Malfunction Summary report: N

BD SAFEASSIST¿ SAFETY PEN NEEDLE

MDR report key: 17231670 · Received June 29, 2023

Report

Report Number
9616656-2023-00672
Event Type
Malfunction
Date Received
June 29, 2023
Date of Event
June 9, 2023
Report Date
July 20, 2023
Manufacturer
BECTON DICKINSON AND CO.
Product Code
FMI
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

H3. 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

H6: INVESTIGATION SUMMARY ONE PHOTO OF A 30G X 8MM SAFE ASSIST CARTON WAS RETURNED FROM LOT. NO. 3010167, CAT. NO. 329917. VISUAL EXAMINATION OF THE RETURNED PHOTO WAS CARRIED OUT AND AN INCORRECT PZN CODE WAS OBSERVED. A LOT HISTORY REVIEW WAS CARRIED OUT AND NO RELATED NON CONFORMANCES WERE RAISED IN ASSOCIATION WITH THIS PACKAGED LOT CONCLUDING ALL INSPECTIONS WERE PERFORMED AS PER THE APPLICABLE OPERATIONS AND MET QC SPECIFICATIONS. THIS COMPLAINT WAS CONFIRMED TO BE A PACKAGING GRAPHICS ERROR THEREFORE A REVIEW OF THE PACKAGING PROCESS AT THE SITE IS NOT REQUIRED. ROOT CAUSE WILL BE DETERMINED AS PART OF A CAPA.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE BD SAFEASSIST¿ SAFETY PEN NEEDLE PZN NUMBER ON THE PRODUCT IS INCORRECT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER COMPLAINED ABOUT WRONG PZN NUMBER ON PRODUCT.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE BD SAFEASSIST¿ SAFETY PEN NEEDLE PZN NUMBER ON THE PRODUCT IS INCORRECT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER COMPLAINED ABOUT WRONG PZN NUMBER ON PRODUCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
309117 BD SAFEASSIST¿ SAFETY PEN NEEDLE HYPODERMIC SINGLE LUMEN NEEDLE FMI BECTON DICKINSON AND CO. 3010167

Patients

Seq Age Sex Outcome Treatment
1 Unknown