| Model Number |
18890 |
| Medical Device Problem Code |
Defective Component (2292)
|
| Health Effect - Clinical Code |
Unintended Extubation (4564)
|
| Date of Event |
06/02/2021
|
|
Type of Reportable Event
|
Malfunction
|
|
Additional Manufacturer Narrative
|
|
If information is provided in the future, a supplemental report will be issued.
|
| |
|
Event or Problem Description
|
|
According to the reporter, during use, the device did not provide necessary sealing.The patient was intubated in an icu ¿ covid and was absolutely necessary to be reintubated.There was no adverse symptoms associated with the tube.
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Search Alerts/Recalls
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