DEVON 31146020

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-01-02 for DEVON 31146020 manufactured by Covidien.

Event Text Entries

[96235024] Submit date: 12/26/17. An investigation is currently under way; upon completion the results will be forwarded. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[96235025] The customer states that the team has found our surgical markers to be bleeding and leaving a jagged line for the incision placement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1282497-2018-00011
MDR Report Key7158399
Date Received2018-01-02
Date of Report2018-08-16
Date Mfgr Received2017-12-03
Date Added to Maude2018-01-02
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 STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524151
Manufacturer G1COVIDIEN
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal Code02048
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameDEVON
Generic NameMARKER, SKIN
Product CodeFZZ
Date Received2018-01-02
Model Number31146020
Catalog Number31146020
Lot Number31146020
Device Expiration Date2019-12-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address15 HAMPSHIRE STREET MANSFIELD MA 02048 US 02048


Patients

Patient NumberTreatmentOutcomeDate
10 2018-01-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.