MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-08-15 for CONAIR WW101GD manufactured by Conair Corporation.
[53044308]
The consumer has agreed to received a new product and the product has not been returned to the manufacturer. Therefore an investigation will not be complete.
Patient Sequence No: 1, Text Type: N, H10
[53044309]
On (b)(6) 2016 the consumer claims that glass on the scale has shattered on the product. No injuries were reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1222304-2016-00033 |
| MDR Report Key | 5876417 |
| Date Received | 2016-08-15 |
| Date of Report | 2016-07-27 |
| Date of Event | 2016-07-27 |
| Date Added to Maude | 2016-08-15 |
| 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 |
| Generic Name | BMI SCALE |
| Product Code | MNW |
| Date Received | 2016-08-15 |
| Model Number | WW101GD |
| Device Availability | N |
| Device Eval'ed by Mfgr | * |
| 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 | 2016-08-15 |