FDA Adverse Event
Summary report: N
JARIT INSULATED LAPAROSCOPIC SPATULA
MDR report key: 7926352
·
Received October 1, 2018
Report
- Report Number
- MW5080279
- Date Received
- October 1, 2018
- Manufacturer
- INTEGRA LIFESCIENCES CORP.
- Product Code
- GAF
- Report Source
- Voluntary report
- Reporter Location
- AL, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
A SPARK OCCURRED IN SURGERY. NO PATIENT HARM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 765075 | JARIT INSULATED LAPAROSCOPIC SPATULA | SPATULA, SURGICAL, GENERAL AND PLASTIC SURGERY | GAF | INTEGRA LIFESCIENCES CORP. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |