LIGACLIP* APPLIER W/MECH STOP Adverse Event — Malfunction (MDR 3005075853-2020-02374)
LIGACLIP* APPLIER W/MECH STOP Adverse Event — Malfunction (MDR 3005075853-2020-02374) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LIGACLIP* APPLIER W/MECH STOP; Generic name: APPLIER, SURGICAL, CLIP; Manufacturer: ETHICON ENDO-SURGERY, LLC..
| Device | LIGACLIP* APPLIER W/MECH STOP |
|---|---|
| Generic name | APPLIER, SURGICAL, CLIP |
| Manufacturer | ETHICON ENDO-SURGERY, LLC. |
| Report number | 3005075853-2020-02374 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | (B)(4). DATE OF EVENT IS 2020. EVENT DAY AND EVENT MONTH WERE NOT REPORTED. INVESTIGATION SUMMARY: THE ANALYSIS RESULTS CONFIRMED THAT THE LX107 DEVICE WAS RETURNED NONFUNCTIONAL AS JAWS WERE FOUND TO BE IN A YIELDED CONDITION THEREFORE, THE CLIPS COULD NOT BE LOADED INTO THE JAWS. POSSIBLE CAUSES FOR THIS CONDITION MAY BE DUE TO THE DEVICE BEING CLOSED OVER AN EXISTING HARD OBJECT OR CLIP, THUS P |
| Source | openFDA MAUDE (device adverse events) |
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