MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-30 for LIGASURE LF5644 manufactured by Covidien Lp.
[185503751]
Device did not fire. Manufacturer response for ligasure, ligasure (per site reporter). Do not see a response from manufacturer.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9897196 |
| MDR Report Key | 9897196 |
| Date Received | 2020-03-30 |
| Date of Report | 2020-03-02 |
| Date of Event | 2019-12-11 |
| Report Date | 2020-03-02 |
| Date Reported to FDA | 2020-03-02 |
| Date Reported to Mfgr | 2020-03-30 |
| Date Added to Maude | 2020-03-30 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | LIGASURE |
| Generic Name | ELECTROSURGICAL, CUTTING COAGULATION ACCESSORIES |
| Product Code | GEI |
| Date Received | 2020-03-30 |
| Returned To Mfg | 2019-12-11 |
| Model Number | LF5644 |
| Catalog Number | LF5644 |
| Lot Number | 92810143X |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | 1 DA |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN LP |
| Manufacturer Address | 15 HAMPSHIRE STREET MANSFIELD MA 02048 US 02048 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-30 |