RAISED TOILET SEAT 1391AP RAISED TOILET SE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2001-01-19 for RAISED TOILET SEAT 1391AP RAISED TOILET SE manufactured by Invacare Corp..

Event Text Entries

[214343] Mfr received a report from a consumer alleging that the raised toilet seat came loose from the commode, causing the user to fall to the floor. As a result of the incident, the consumer sustained injuries to the head requiring stitches and abrasion to the forearm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1525712-2000-00107
MDR Report Key313609
Report Source04
Date Received2001-01-19
Date of Report2000-12-31
Date of Event2000-09-08
Date Mfgr Received2000-09-29
Date Added to Maude2001-01-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactRAE FARROW
Manufacturer Street899 CLEVELAND ST.
Manufacturer CityELYRIA OH 44035
Manufacturer CountryUS
Manufacturer Postal44035
Manufacturer Phone4403296356
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRAISED TOILET SEAT
Generic NameDAILY ACTIVITY ASSIST DEVICE
Product CodeIKW
Date Received2001-01-19
Model NumberRAISED TOILET SEAT
Catalog Number1391AP RAISED TOILET SE
Lot NumberNA
ID NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key303302
ManufacturerINVACARE CORP.
Manufacturer Address899 CLEVELAND ST ELYRIA OH 44035 US
Baseline Brand NameCOMMODE
Baseline Generic NameDAILY ACTIVITY ASSIST DEVICE
Baseline Model NoRAISED TOILET S
Baseline Catalog NoRAISED TOILET SEAT
Baseline IDNA
Baseline Device FamilyDAILY ACTIVITY ASSIST DEVICE
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2001-01-19

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