FDA Adverse Event Malfunction Summary report: N

HUDSON MICRO MIST NEBULIZER W/TEE, MOUTHPIECE

MDR report key: 2171437 · Received June 29, 2011

Report

Report Number
3004365956-2011-00267
Event Type
Malfunction
Date Received
June 29, 2011
Date of Event
February 1, 2011
Report Date
June 22, 2011
Manufacturer
TELEFLEX MEDICAL
Product Code
CAF
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

NO SAMPLE IS AVAILABLE FOR THE MANUFACTURER TO EVALUATE. A FOLLOW-UP REPORT WILL BE SENT WHEN INVESTIGATION IS COMPLETED.

Description of Event or Problem · 1

THE EVENT IS REPORTED AS: COMPLAINT ALLEGES: THE PEDIATRIC HEAD NURSE REPORTED THAT A (B)(6) BABY GIRL WAS RECEIVING ATOMIZATION TREATMENT WHEN SHE PULLED THE NOSE CLIP OFF BECAUSE SHE DIDN'T WANT TREATMENT, AND THERE WAS A SHARP METAL BURR THAT STABBED THE PTS HAND. THE NURSE WAS ABLE TO QUICKLY DISINFECT THE WOUND AND THE PT IS CURRENTLY IN GOOD CONDITION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HUDSON MICRO MIST NEBULIZER W/TEE, MOUTHPIECE NEBULIZER CAF TELEFLEX MEDICAL NA UNK

Patients

Seq Age Sex Outcome Treatment
1 14 MO