MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-05-17 for V. MUELLER BRUNS * NL 6760-006 manufactured by Carefusion.
[1555155]
While surgeon was performing a left knee arthroplasty, the curette tip broke off. Curette tip was retrieved, there was no harm to the patient.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1694411 |
| MDR Report Key | 1694411 |
| Date Received | 2010-05-17 |
| Date of Report | 2010-05-17 |
| Date of Event | 2010-05-17 |
| Report Date | 2010-05-17 |
| Date Reported to FDA | 2010-05-17 |
| Date Added to Maude | 2010-05-20 |
| 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 | V. MUELLER BRUNS |
| Generic Name | CURETTE |
| Product Code | FZS |
| Date Received | 2010-05-17 |
| Model Number | * |
| Catalog Number | NL 6760-006 |
| Lot Number | * |
| ID Number | * |
| Operator | PHYSICIAN |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAREFUSION |
| Manufacturer Address | 1240 WAUKEGAN RD. PARK CITY IL 60085 US 60085 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2010-05-17 |