MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2011-07-14 for TINCOCO manufactured by .
[2127233]
I had bought a tincoco compression legwear which does not fit the description, it does not "tight" as normal like socks. But the seller claim that it is real and refuse to refund or change good to me. This is my second time to buy tincoco. First time was with another person, it is good to wear and very tight, but this second time with another seller, left me disappointed and sad. Dates of use: (b)(6) 2011.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5021417 |
| MDR Report Key | 2172038 |
| Date Received | 2011-07-14 |
| Date of Report | 2011-07-14 |
| Date of Event | 2011-07-12 |
| Date Added to Maude | 2011-07-26 |
| 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 | 0 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | TINCOCO |
| Generic Name | TINCOCO COMPRESSION LEGWEAR 980D |
| Product Code | DWL |
| Date Received | 2011-07-14 |
| Lot Number | JY-1066 ??? |
| ID Number | FDA880.5780, 8310561258 |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2011-07-14 |