FDA Adverse Event
Other
Summary report: N
AESCULAP
MDR report key: 23497063
·
Received November 7, 2025
Report
- Report Number
- MW5178606
- Event Type
- Other
- Date Received
- November 7, 2025
- Report Date
- October 31, 2025
- Manufacturer
- AESCULAP INC.
- Product Code
- GDZ
- Report Source
- Voluntary report
- Reporter Occupation
- UNKNOWN
- Health Professional
- *
Narratives
Description of Event or Problem · 0
KNIFE HANDLE BROKE OFF.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2177602 | AESCULAP | HANDLE, SCALPEL | GDZ | AESCULAP INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |