GOWN, SURGICAL L3 740* 7400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-11-21 for GOWN, SURGICAL L3 740* 7400 manufactured by Novo Health Services.

MAUDE Entry Details

Report Number1000306225-2019-00005
MDR Report Key9360111
Report SourceUSER FACILITY
Date Received2019-11-21
Date of Report2019-11-29
Date of Event2019-10-31
Date Mfgr Received2019-10-31
Date Added to Maude2019-11-21
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 ContactMS. ZILLERY FORTNER
Manufacturer Street7086 INDUSTRIAL ROW DRIVE
Manufacturer CityMASON OH 45040
Manufacturer CountryUS
Manufacturer Postal45040
Manufacturer Phone5133986406
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGOWN, SURGICAL L3
Generic NameREUSABLE LEVEL III SURGICAL GOWN
Product CodeFYA
Date Received2019-11-21
Model Number740*
Catalog Number7400
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNOVO HEALTH SERVICES
Manufacturer Address6024 CENTURY OAKS DR CHATTANOOGA TN 37416 US 37416


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-11-21

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