MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1997-07-03 for OCL SPLINT UNK manufactured by Ocl.
[20997383]
Pt experienced redness and rash where the splint had contact with the skin. This was experienced 72 hours after the application of the splint.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1011617 |
| MDR Report Key | 102890 |
| Date Received | 1997-07-03 |
| Date of Report | 1997-07-03 |
| Date of Event | 1997-06-30 |
| Date Added to Maude | 1997-07-08 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | OCL SPLINT |
| Generic Name | SPLINT |
| Product Code | ILH |
| Date Received | 1997-07-03 |
| Model Number | UNK |
| Catalog Number | UNK |
| Lot Number | 80482 |
| ID Number | CS215-REORDER# |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 101256 |
| Manufacturer | OCL |
| Manufacturer Address | UNK UNK * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1997-07-03 |