FDA Adverse Event Malfunction Summary report: N

LEVEL 1

MDR report key: 12362806 · Received August 24, 2021

Report

Report Number
3012307300-2021-08813
Event Type
Malfunction
Date Received
August 24, 2021
Date of Event
January 22, 2021
Report Date
August 24, 2021
Product Code
LGZ
UDI-DI
40695085401002
PMA / PMN Number
K911383
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION COMPLETED ON A SMITHS MEDICAL FLUID WARMING/LEVEL 1 HOTLINE ACCESSORIES WITH TWO PICTURES ATTACHED FOR EVALUATION. THE RESULTS FROM THE PICTURES REVEAL LIQUID IN THE FILTER. DURING TESTING WITH SAMPLE UNIT, IT WAS DISCOVERED LEAKING DETECTED IN VALVE DISC. AFTER SAMPLE EVALUATION THE MOST PROBABLE ROOT CAUSE FOR THE LEAK CONDITION IN VALVE DISC IS DUE TO A OPERATOR OVERSIGHT THE OPERATION ADHESIVE (LOCTITE 495) IN THE VALVE DISC, DURING DISC APPLICATION PROCESS, PROCEDURE MP L-10 OPERATION 4.7 USING LOCTITE 495 AND EFD SOLVENT DISPENSER (1000SERIES), STEP ON FOOT PEDAL TO APPLY SINGLE DROPLET OF LOCTITE 495 TO CENTER OF VENT DISC SEAT OR CASTLE RING ON GAS VENT BODY WAS NOT CORRECTLY FOLLOWED. AN AWARENESS NOTIFICATION WAS CONDUCTED BY THE QUALITY ENGINEER TO THE PRODUCTION PERSONNEL IN ORDER TO AVOID THE OVERSIGHT THE ADHESIVE OPERATION. CUSTOMER CONTACT PHONE NUMBER: (B)(6). CUSTOMER FACILITY PHONE NUMBER: (B)(6). DEVICE EVALUATION IN PROGRESS.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE GAS VENT WAS LEAKING FLUID FROM THE FILTER. THE PRODUCT PROBLEM WAS OBSERVED DURING PATIENT USE. THE PRODUCT FAULT DID NOT CAUSE OR CONTRIBUTE TO ANY ADVERSE PATIENT HEALTH EFFECTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1260377 LEVEL 1 WARMER, THERMAL, INFUSION FLUID LGZ L-10 4016708 40695085401002

Patients

Seq Age Sex Outcome Treatment
1