ENDOPATH ENDOSCOPIC LINEAR CUTTER Adverse Event — Malfunction (MDR 1527736-1997-01361)
ENDOPATH ENDOSCOPIC LINEAR CUTTER Adverse Event — Malfunction (MDR 1527736-1997-01361) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENDOPATH ENDOSCOPIC LINEAR CUTTER; Generic name: ENDOSCOPIC LINEAR CUTTER; Manufacturer: ETHICON ENDO-SURGERY, INC..
| Device | ENDOPATH ENDOSCOPIC LINEAR CUTTER |
|---|---|
| Generic name | ENDOSCOPIC LINEAR CUTTER |
| Manufacturer | ETHICON ENDO-SURGERY, INC. |
| Report number | 1527736-1997-01361 |
| Event type | Malfunction |
| Date received | 1997-06-20 |
| Report source | Company representation |
| Narrative | THE PRODUCT COMPLAINT ANALYSIS TEAM HAS COMPLETED ITS INVESTIGATION OF THE DEVICE WHICH WAS RETURNED TO CO WITH PRODUCT INQUIRY #973145. VISUAL INSPECTIONS & RESULTS: LOCKOUT POSITION, FIRED; CARTRIDGE CONDITION, 1/4 FIRED AND CARTRIDGE RETURN BATCH NUMBER, K00P98. FUNCTIONAL TESTS & RESULTS: CONDITION OF FIRING TRIGGER LOCKOUT, GOOD; CONDITION OF PINION GEAR, BROKEN; CONDITION OF SHORT RACK, GOOD |
| Source | openFDA MAUDE (device adverse events) |
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