MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2006-07-28 for #10 PRE-MADE PACK * manufactured by Bd Vendor.
[19150711]
#10 knife blade broke while dr. Was using it. Pieces recovered and placed in specimen cup labeled with pt info. Risk mgmt has the specimen.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 742952 |
| MDR Report Key | 742952 |
| Date Received | 2006-07-28 |
| Date of Report | 2006-07-10 |
| Date of Event | 2006-05-22 |
| Date Facility Aware | 2006-05-22 |
| Report Date | 2006-07-10 |
| Date Added to Maude | 2006-08-03 |
| 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 | 3 |
| Reporter Occupation | RISK MANAGER |
| 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 | #10 PRE-MADE PACK |
| Generic Name | KNIFE |
| Product Code | EMF |
| Date Received | 2006-07-28 |
| Model Number | #10 PRE-MADE PACK |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 730760 |
| Manufacturer | BD VENDOR |
| Manufacturer Address | ONE BECTON DR. FRANKLINE LAKE NJ * US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2006-07-28 |