MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2011-05-09 for * R6/10 CODMAN 44 32-3473 STAINLESS 0 manufactured by Codman & Shurtleff, Inc..
[1983664]
A #0 currette broke off in patient. Broken piece was removed. Incision had to be enlarged because it broke.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2092280 |
| MDR Report Key | 2092280 |
| Date Received | 2011-05-09 |
| Date of Report | 2011-05-09 |
| Date of Event | 2011-05-04 |
| Report Date | 2011-05-09 |
| Date Reported to FDA | 2011-05-09 |
| Date Added to Maude | 2011-05-18 |
| 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 | * |
| Generic Name | CURETTE, SURGICAL, GENERAL USE |
| Product Code | FZS |
| Date Received | 2011-05-09 |
| Model Number | R6/10 |
| Catalog Number | CODMAN 44 32-3473 STAINLESS 0 |
| Lot Number | * |
| ID Number | * |
| Operator | PHYSICIAN |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CODMAN & SHURTLEFF, INC. |
| Manufacturer Address | 325 PARAMOUNT DR. RAYNHAM MA 02767 US 02767 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2011-05-09 |