MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2003-08-25 for UNK manufactured by Unk.
[18146961]
Removal of 2 k-wires.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 480407 |
MDR Report Key | 480407 |
Date Received | 2003-08-25 |
Date of Report | 2003-08-25 |
Date of Event | 2003-08-07 |
Date Facility Aware | 2003-08-07 |
Report Date | 2003-08-25 |
Date Reported to FDA | 2003-08-25 |
Date Added to Maude | 2003-08-29 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNK |
Generic Name | UNK |
Product Code | DZK |
Date Received | 2003-08-25 |
Model Number | UNK |
Catalog Number | UNK |
Lot Number | UNK |
ID Number | UNK |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | UNKNOWN |
Implant Flag | Y |
Date Removed | V |
Device Sequence No | 1 |
Device Event Key | 469254 |
Manufacturer | UNK |
Manufacturer Address | UNK UNK * |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2003-08-25 |