MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-08-16 for CONAIR CORPORATION WW705 manufactured by Conair Corporation.
[53052454]
On 8/16/2016 - per our risk management team, no injuries or property damaged occured. The consumer has agreed to receive a replacement product and discarded the original product. Therefore, an investigation is not necessary. Device not returned to manufacturer.
Patient Sequence No: 1, Text Type: N, H10
[53052455]
On 7/12/2016 - the consumer claims that the glass on the product shattered while in use. No injuries occurred
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1222304-2016-00032 |
| MDR Report Key | 5879493 |
| Date Received | 2016-08-16 |
| Date of Report | 2016-07-19 |
| Date of Event | 2016-07-18 |
| Date Added to Maude | 2016-08-16 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Street | 1 CUMMINGS POINT RD. |
| Manufacturer City | STAMFORD CT 06902 |
| Manufacturer Country | US |
| Manufacturer Postal | 06902 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | CONAIR CORPORATION |
| Generic Name | SCALE |
| Product Code | MNW |
| Date Received | 2016-08-16 |
| Model Number | WW705 |
| Device Availability | * |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CONAIR CORPORATION |
| Manufacturer Address | 1 CUMMINGS POINT RD STAMFORD CT 06902 US 06902 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2016-08-16 |