FDA Adverse Event
Malfunction
Summary report: N
TELEFLEX LMA #3
MDR report key: 23631440
·
Received November 24, 2025
Report
- Report Number
- MW5179342
- Event Type
- Malfunction
- Date Received
- November 24, 2025
- Date of Event
- November 18, 2025
- Report Date
- November 19, 2025
- Manufacturer
- TELEFLEX MEDICAL LLC.
- Product Code
- CAE
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- US
- Reporter Occupation
- NURSE
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
ANESTHESIOLOGISTS FREQUENTLY FIND THE PRODUCT WILL NOT FULLY DEFLATE AFTER USE AND PRIOR TO REMOVAL FROM PATIENT MOUTH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2578047 | TELEFLEX LMA #3 | AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY | CAE | TELEFLEX MEDICAL LLC. | 105200-000030 | 11F25D0169 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown | Other |