MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-05-27 for TANNING BED manufactured by Unk.
[76536975]
(b)(6) in (b)(6) sold me a membership. After tanning 4 times i realized a skin rash started on back. I noticed while tanning the beds were filthy under the lip of the glass and the fans that blow in your face were full of dust and dead flies were under the glass of the bed. I also was not given eye protection upon entering the room to tan.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5070123 |
| MDR Report Key | 6604636 |
| Date Received | 2017-05-27 |
| Date of Report | 2017-05-27 |
| Date of Event | 2017-05-15 |
| Date Added to Maude | 2017-06-01 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| 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 | TANNING BED |
| Generic Name | TANNING BED |
| Product Code | REF |
| Date Received | 2017-05-27 |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Brand Name | TANNING BED |
| Generic Name | TANNING BED |
| Product Code | REF |
| Date Received | 2017-05-27 |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 2 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Brand Name | TANNING BED |
| Generic Name | TANNING BED |
| Product Code | REF |
| Date Received | 2017-05-27 |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 3 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-05-27 |