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 |