FDA Adverse Event Malfunction Summary report: N

PN RELION 32G X 4MM 3B TW

MDR report key: 11986976 · Received June 11, 2021

Report

Report Number
3014704491-2021-00023
Event Type
Malfunction
Date Received
June 11, 2021
Date of Event
May 18, 2021
Report Date
June 18, 2021
Manufacturer
BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU
Product Code
FMI
PMA / PMN Number
K162516
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

H6: INVESTIGATION SUMMARY: NO SAMPLES (INCLUDING PHOTOS) WERE RETURNED THEREFORE THE COMPLAINT COULD NOT BE CONFIRMED AND THE ROOT CAUSE IS UNDETERMINED. CLOG TEST WAS CONDUCTED ON 7PCS RETENTION SAMPLES AND NO NEEDLE CLOG FAIL FOUND. THIS IS THE 2ND COMPLAINT FOR THE REPORTED LOT NUMBER. A REVIEW OF THE MANUFACTURING RECORDS WAS PERFORMED AND NO NON-CONFORMANCES WERE RAISED IN ASSOCIATION WITH THIS TYPE OF EVENT FOR THIS LOT.

Description of Event or Problem · 0

IT WAS REPORTED THAT 1 PN RELION 32G X 4MM 3B TW NEEDLE WAS UNABLE OR DIFFICULT TO PRIME. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER : IT WAS REPORTED BY THE CONSUMER THAT THE PEN NEEDLES CLOG DURING PRIMING. DATE OF EVENT: UNKNOWN. SAMPLES: DISCARDED.

Additional Manufacturer Narrative · 1

DATE OF EVENT: UNKNOWN. THE DATE RECEIVED BY MANUFACTURER HAS BEEN USED FOR THIS FIELD. A DEVICE EVALUATION IS PENDING BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Description of Event or Problem · 1

IT WAS REPORTED THAT 1 PN RELION 32G X 4MM 3B TW NEEDLE WAS UNABLE OR DIFFICULT TO PRIME. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER : IT WAS REPORTED BY THE CONSUMER THAT THE PEN NEEDLES CLOG DURING PRIMING. DATE OF EVENT: UNKNOWN. SAMPLES: DISCARDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
878414 PN RELION 32G X 4MM 3B TW HYPODERMIC SINGLE LUMEN NEEDLE FMI BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU 0136694

Patients

Seq Age Sex Outcome Treatment
1