MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-06-24 for HYPERBARIC CHAMBER VITAERIS 320 manufactured by Oxyhealth, Llc.
[78598668]
I have a vitaeris 320 from oxyhealth. I turned it on and after full pressure the big window exploded in the corner and all the air came out.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5070651 |
| MDR Report Key | 6669642 |
| Date Received | 2017-06-24 |
| Date of Report | 2017-06-24 |
| Date of Event | 2017-06-18 |
| Date Added to Maude | 2017-06-27 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | HYPERBARIC CHAMBER |
| Generic Name | HYPERBARIC CHAMBER |
| Product Code | CBF |
| Date Received | 2017-06-24 |
| Model Number | VITAERIS 320 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | OXYHEALTH, LLC |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2017-06-24 |