FDA Adverse Event Malfunction Summary report: N

TAP III

MDR report key: 2192761 · Received June 9, 2011

Report

Report Number
3003496134-2011-00027
Event Type
Malfunction
Date Received
June 9, 2011
Date of Event
May 1, 2011
Report Date
June 2, 2011
Manufacturer
AIRWAY MANAGEMENT INC.
Product Code
LRK
PMA / PMN Number
K062951
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
DENTIST

Narratives

Additional Manufacturer Narrative · 1

AMI HAS REPAIRED THE APPLIANCE AND REPLACED THE LOWER TRAY. (B)(4).

Description of Event or Problem · 1

DENTIST CONTACTED AMI AND STATED THAT THE UPPER HARDWARE HAS BROKEN OFF THE UPPER APPLIANCE. THERE WAS NO HARM TO THE PT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TAP III SLEEP APNEA DEVICE LRK AIRWAY MANAGEMENT INC. 12TL-00GE-11

Patients

Seq Age Sex Outcome Treatment
1