FDA Adverse Event
Malfunction
Summary report: N
PROXIMATE PLUS MD MULTI-DIRECTIONAL RELEASE SKIN STAPLER - 35 WIDE
MDR report key: 1320830
·
Received February 24, 2009
Report
- Report Number
- 3005075853-2008-03441
- Event Type
- Malfunction
- Date Received
- February 24, 2009
- Date of Event
- November 6, 2008
- Report Date
- November 10, 2008
- Manufacturer
- ETHICON ENDO-SURGERY, LLC
- Product Code
- GDT
- PMA / PMN Number
- K833357
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
DATE SENT: 12/03/2008. INFO ANTICIPATED, BUT UNAVAILABLE AT THIS TIME.
Description of Event or Problem · 1
IT WAS REPORTED THAT DURING A GASTRECTOMY PROCEDURE, THE STAPLE CAME OUT CROOKED. ANOTHER DEVICE WAS USED TO COMPLETE THE CASE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PROXIMATE PLUS MD MULTI-DIRECTIONAL RELEASE SKIN STAPLER - 35 WIDE | NONE | GDT | ETHICON ENDO-SURGERY, LLC | NA | E4LX3Z |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |