MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2016-02-24 for CONAIR SCALE WW707 manufactured by Conair Corporation.
[38960513]
On 2/9/2016 - risk management team has attempted to contact the consumer on three occasions to assist in this matter and retrieve the product for evaluation. To date, the consumer has not responded. Device not returned to manufacturer.
Patient Sequence No: 1, Text Type: N, H10
[38960514]
Consumer alleges to have cut her thumb while cleaning the product. Consumer seeked medical attention for her injury.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1222304-2016-00014 |
| MDR Report Key | 5457486 |
| Report Source | CONSUMER |
| Date Received | 2016-02-24 |
| Date of Report | 2016-02-02 |
| Date of Event | 2016-01-20 |
| Date Added to Maude | 2016-02-24 |
| 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 | 3 |
| Brand Name | CONAIR SCALE |
| Generic Name | WW707 SCALE |
| Product Code | MNW |
| Date Received | 2016-02-24 |
| Model Number | WW707 |
| 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. Hospitalization | 2016-02-24 |