MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2016-02-26 for CONAIR SCALE manufactured by Conair Corporation.
[39158888]
On (b)(6) 2016: - the consumer has discarded the device. Therefore, an evaluation will not be possible. Consumer has requested a replacement. A replacement will be sent to the consumer once photos of purchase has been received.
Patient Sequence No: 1, Text Type: N, H10
[39158889]
On (b)(6) 2016 - consumer alleges the glass on the scale exploded when placed on the floor. The consumer received cuts on hands and feet. The scale was discarded. Consumer will submit photos as proof of purchase. The consumer has requested a replacement.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1222304-2016-00015 |
| MDR Report Key | 5463925 |
| Report Source | CONSUMER |
| Date Received | 2016-02-26 |
| Date of Report | 2016-02-17 |
| Date of Event | 2016-02-17 |
| Date Added to Maude | 2016-02-26 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 3 |
| 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 | 3 |
| Brand Name | CONAIR SCALE |
| Generic Name | BMI SCALE |
| Product Code | MNW |
| Date Received | 2016-02-26 |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 0 |
| 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 | 2016-02-26 |