MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-09-28 for DIAMOND TANNING BED manufactured by Unk.
[122334008]
I went to tanning salon and asked specifically to be used a tanning bed that does not burn skin. I was concerned about my skin burning. I was told to buy the most expensive package to use their most expensive tanning beds, and that i would not get burned. The associate and i believe a mgr confirmed this. I went into their bed for 10 mins and within 12 hours my abdomen and front legs are severely sunburned. I went back the day after and told the same associate what happened. She said she did not know why it happened, that i heard her mgr say the bed did not use burning type bulbs. I asked for my money back. The associate first said they don't print receipts, then she printed something that said my membership had been cancelled. That's not a refund. (b)(6).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5080226 |
| MDR Report Key | 7922548 |
| Date Received | 2018-09-28 |
| Date of Report | 2018-09-28 |
| Date of Event | 2018-09-26 |
| Date Added to Maude | 2018-10-01 |
| 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 | DIAMOND TANNING BED |
| Generic Name | BOOTH, SUN TAN |
| Product Code | LEJ |
| Date Received | 2018-09-28 |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Deathisabilit | 2018-09-28 |