MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2007-07-26 for V MUELLER manufactured by V Mueller.
[19895339]
Tip of nerve hook broke off while in use. Retrieved in suction cannister.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5003188 |
| MDR Report Key | 887569 |
| Date Received | 2007-07-26 |
| Date of Report | 2007-07-26 |
| Date of Event | 2007-07-25 |
| Date Added to Maude | 2007-08-10 |
| 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 | 3 |
| Reporter Occupation | RISK MANAGER |
| 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 | V MUELLER |
| Generic Name | MICRONERVE HOOK |
| Product Code | GZX |
| Date Received | 2007-07-26 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 868722 |
| Manufacturer | V MUELLER |
| Manufacturer Address | 7000 CARDINAL PLACE DUBLIN OH 43017 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2007-07-26 |