MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-31 for LIGASURE LF2019 manufactured by Covidien Mfg Dc Boulder.
[185708156]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[185708157]
According to the reporter, during a thyroidectomy procedure, the devices' jaws broke and tiny pieces fell on the cavity and on the or (operating room) table but were retrieved. There was no patient injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1717344-2020-00355 |
MDR Report Key | 9902033 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-03-02 |
Date Mfgr Received | 2020-03-02 |
Device Manufacturer Date | 2019-08-20 |
Date Added to Maude | 2020-03-31 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
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 |
Manufacturer Contact | LISA HERNANDEZ |
Manufacturer Street | 5920 LONGBOW DRIVE |
Manufacturer City | BOULDER CO 80301 |
Manufacturer Country | US |
Manufacturer Postal | 80301 |
Manufacturer Phone | 2034925563 |
Manufacturer G1 | COVIDIEN MFG DC BOULDER |
Manufacturer Street | 5920 LONGBOW DR |
Manufacturer City | BOULDER CO 803013299 |
Manufacturer Country | US |
Manufacturer Postal Code | 803013299 |
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 | 2020-03-31 |
Model Number | LF2019 |
Catalog Number | LF2019 |
Lot Number | 92170142X |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN MFG DC BOULDER |
Manufacturer Address | 5920 LONGBOW DR BOULDER CO 803013299 US 803013299 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-31 |