VISTEC SPG 4X4 STR 10S 16 PLY 7317

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-12-08 for VISTEC SPG 4X4 STR 10S 16 PLY 7317 manufactured by Covidien.

Event Text Entries

[62331313] An investigation is currently underway. Upon completion, the results will be forwarded.
Patient Sequence No: 1, Text Type: N, H10


[62331314] It was reported to covidien on (b)(6) 2016 that a customer had an issue with a gauze sponge. The customer states they received 12 sponges instead of 10.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018120-2016-00177
MDR Report Key6155758
Date Received2016-12-08
Date of Report2016-11-30
Date Mfgr Received2016-11-30
Date Added to Maude2016-12-08
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 Street1430 MARVIN GRIFFIN ROAD
Manufacturer CityAUGUSTA GA 30906
Manufacturer CountryUS
Manufacturer Postal Code30906
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameVISTEC SPG 4X4 STR 10S 16 PLY
Generic NameGAUZE SPONGE
Product CodeEFQ
Date Received2016-12-08
Model Number7317
Catalog Number7317
Lot Number16C033362
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address1430 MARVIN GRIFFIN ROAD AUGUSTA GA 30906 US 30906


Patients

Patient NumberTreatmentOutcomeDate
10 2016-12-08

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