LigaSure · ELECTROSURGICAL, CUTTING & COAGULATION & ACCES
Covidien · Retraction Problem, Protective Measures Problem
- Manufacturer contact zip ext
- -439
- Manufacturer contact state
- MN
- Manufacturer link flag
- Y
- Manufacturer g1 city
- BOULDER
- Manufacturer contact address 1
- 8200 Coral Sea St NE
- Manufacturer contact pcity
- +1(800)6
- Event type
- Malfunction
- Report number
- 1717344-2026-01329
- Product problem flag
- Y
- Date received
- 20260930
- PMA pmn number
- K173281
- Date of event
- 20260911
- Reprocessed and reused flag
- N
- Manufacturer contact zip code
- 55112
- Reporter occupation code
- OTHER HEALTH CARE PROFESSIONAL
- Manufacturer contact plocal
- +1(800)646-4633
- Noe summarized
- 1
- Manufacturer contact l name
- Bocchino
- Manufacturer g1 postal code
- 80301-3299
- Manufacturer g1 state
- CO
- Reporter country code
- TW
- Date added
- 20260930
- Manufacturer contact f name
- Mike
- Device date of manufacturer
- 20251202
- Previous use code
- I
- Mfr report type
- Thirty-Day
- Manufacturer contact country
- US
- Date changed
- 20260930
- Health professional
- Y
- Summary report flag
- N
- Manufacturer g1 zip code ext
- -329
- Date report
- 20260929
- Initial report to FDA
- No
- Manufacturer g1 country
- US
- Manufacturer contact city
- Mounds View
- MDR report key
- 50941440
- Date manufacturer received
- 20260911
- Report source code
- Manufacturer report
- Manufacturer g1 zip code
- 80301
- Manufacturer g1 name
- Covidien
- Adverse event flag
- N
- Single use flag
- Y
- Manufacturer g1 address 1
- 6044 Longbow Court
- Manufacturer contact postal code
- 55112-4391
- Type of report
- Initial submission
- Source type
- Foreign, Health Professional, Company representation
- Device
- Device sequence number
- 319552
- Serviced by 3rd party flag
- N
- Date received
- 20260930
- Brand name
- LigaSure
- Generic name
- ELECTROSURGICAL, CUTTING & COAGULATION & ACCES
- Manufacturer d name
- Covidien
- Manufacturer d address 1
- 6044 Longbow Court
- Manufacturer d city
- BOULDER
- Manufacturer d state
- CO
- Manufacturer d zip code
- 80301
- Manufacturer d zip code ext
- -329
- Manufacturer d country
- US
- Manufacturer d postal code
- 80301-3299
- Device operator
- HEALTH PROFESSIONAL
- Model number
- LF2019
- Catalog number
- LF2019
- Lot number
- 53360306X
- Device availability
- No
- Device report product code
- GEI
- Combination product flag
- N
- UDI di
- 10884521741096
- UDI public
- (01)10884521741096(17)301201(10)53360306X
- Harmonized identifiers (openFDA)
- Device name
- Electrosurgical, Cutting & Coagulation & Accessories
- Medical specialty description
- General, Plastic Surgery
- Regulation number
- 878.4400
- Device class
- 2
- Product problems
- Retraction Problem, Protective Measures Problem
- Patient
- Patient sequence number
- 1
- Date received
- 20260930
- Patient sex
- Unknown
- Patient problems
- No Clinical Signs, Symptoms or Conditions