SMITHS MEDICAL PORTEX COMBINED SPINAL EPIDURAL TRAY A3307-17

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-02-28 for SMITHS MEDICAL PORTEX COMBINED SPINAL EPIDURAL TRAY A3307-17 manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[181408065] Information was received that a smiths medical epidural tray had a hole in the side wall of the catheter and fluid was noted to have leaked out. No adverse effects reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-01608
MDR Report Key9770052
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-02-28
Date of Report2020-03-31
Date Mfgr Received2020-03-31
Date Added to Maude2020-02-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactDAVE HALVERSON
Manufacturer Street6000 NATHAN LANE N
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer G1SMITHS MEDICAL ASD, INC.
Manufacturer Street10 BOWMAN DRIVE
Manufacturer CityKEENE, NH
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSMITHS MEDICAL PORTEX COMBINED SPINAL EPIDURAL TRAY
Generic NameSPINAL EPIDURAL ANESTHESIA KIT
Product CodeOFT
Date Received2020-02-28
Catalog NumberA3307-17
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE N MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-28

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