3611 LITE GLOVE 31140208

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-01-23 for 3611 LITE GLOVE 31140208 manufactured by Covidien.

Event Text Entries

[65830293] Submit date: 01/23/2017. An investigation is currently underway. Upon completion, the results will be forwarded.
Patient Sequence No: 1, Text Type: N, H10


[65830294] It was reported to covidien on (b)(6) 2016 that an issue occurred with a lite glove. The light glove tore during the surgery. There was no harm to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9612030-2017-00029
MDR Report Key6269510
Date Received2017-01-23
Date of Report2016-12-29
Date of Event2016-11-07
Date Mfgr Received2016-12-29
Date Added to Maude2017-01-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactEDWARD ALMEIDA
Manufacturer Street15 HAMPSHIRE ST
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524151
Manufacturer G1COVIDIEN
Manufacturer StreetCALLE 9 SUR NO. 125 CUIDAD INDUSTRIAL
Manufacturer CityTIJUANA
Manufacturer CountryMX
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand Name3611 LITE GLOVE
Generic NameLITE GLOVE
Product CodeLYU
Date Received2017-01-23
Model Number31140208
Catalog Number31140208
Lot Number6162100264
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressCALLE 9 SUR NO. 125 CUIDAD INDUSTRIAL TIJUANA MX


Patients

Patient NumberTreatmentOutcomeDate
10 2017-01-23

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