ENDOPATH*PROBE PLUS II SHAFT Adverse Event — Malfunction (MDR 3005075853-2020-02402)
ENDOPATH*PROBE PLUS II SHAFT Adverse Event — Malfunction (MDR 3005075853-2020-02402) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENDOPATH*PROBE PLUS II SHAFT; Generic name: LAPAROSCOPE, GENERAL AND PLASTIC SURGERY; Manufacturer: ETHICON ENDO-SURGERY, LLC..
| Device | ENDOPATH*PROBE PLUS II SHAFT |
|---|---|
| Generic name | LAPAROSCOPE, GENERAL AND PLASTIC SURGERY |
| Manufacturer | ETHICON ENDO-SURGERY, LLC. |
| Report number | 3005075853-2020-02402 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN, OTHER |
| Narrative | (B)(4). BATCH #UNK. AS THE DEVICE WAS NOT RETURNED, AN ANALYSIS INVESTIGATION COULD NOT BE PERFORMED. A CONCLUSION COULD NOT BE REACHED AS TO WHAT MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT. COMPLAINT INFORMATION IS TRENDED ON A REGULAR BASIS TO DETERMINE IF FURTHER INVESTIGATION IS WARRANTED. THE LOT/ BATCH WAS NOT PROVIDED; THEREFORE, THE MANUFACTURING RECORDS EVALUATION COULD NOT BE PERFORMED. |
| Source | openFDA MAUDE (device adverse events) |
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