MAUDE Adverse Event Report: TELEFLEX MEDICAL HUDSON MICROMIST NEBULIZER,W/IN-LINE NEBTEE VL; NEBULIZER (DIRECT PATIENT INTE

Catalog Number 41745

Device Problem Fitting Problem (2183)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Date 10/11/2019

Event Type  malfunction  

Manufacturer Narrative

(b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.A visual inspection of the product involved in the complaint was performed on two pictures provided by the customer of two components that are part of product code 1883 (micro mist nebulizer w/tee, tbg & mthpc).Customer complaint is not related to a visual issue it is related to a dimensional defect, no visual issues can be observed that can lead to this customer complaint.A device history record review was performed and no relevant findings were identified.Without the device to evaluate, the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.If the sample becomes available at a later date a follow up report will be submitted with investigation results.

Event Description

Customer reported the "the connector is large does not fit".It was reported that the alleged issue was discovered when connecting the tubing to the nebulizer.No patient harm reported.

• Brand Name: HUDSON MICROMIST NEBULIZER,W/IN-LINE NEBTEE VL
• Type of Device: NEBULIZER (DIRECT PATIENT INTE
• Manufacturer (Section D): TELEFLEX MEDICAL; morrisville NC
• Manufacturer (Section G): TELEFLEX MEDICAL; parque industrial finsa; nuevo laredo 88275 ; MX 88275
• Manufacturer Contact: victoria sandlin ; 3015 carrington mill blvd; morrisville, NC 27560
• MDR Report Key: 9281424
• MDR Text Key: 194830011
• Report Number: 3004365956-2019-00319
• Device Sequence Number: 1
• Product Code: CAF
• Combination Product (y/n): N
• Reporter Country Code: SF
• PMA/PMN Number: K930525
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 10/16/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/05/2019
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Device Expiration Date: 10/31/2023
• Device Catalogue Number: 41745
• Device Lot Number: 74L1800203
• Was Device Available for Evaluation?: Yes
• Date Manufacturer Received: 10/16/2019
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 11/01/2018
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1