STAIR PRO - MODEL 6252 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2009-08-31 for STAIR PRO - MODEL 6252 NA manufactured by Stryker Corp, Medical Division.

Event Text Entries

[1137061] It was reported that the chair would not grip on bare wood floors. No pt involvement or adverse consequence is alleged.
Patient Sequence No: 1, Text Type: D, B5


[8315303] Na
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1831750-2009-00916
MDR Report Key1463375
Report Source07
Date Received2009-08-31
Date of Report2008-01-07
Date of Event2008-01-07
Date Mfgr Received2008-01-07
Device Manufacturer Date2005-10-15
Date Added to Maude2009-12-22
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactRENATA SILA
Manufacturer Street3800 E. CENTRE AVE.
Manufacturer CityPORTAGE MI 49002
Manufacturer CountryUS
Manufacturer Postal49002
Manufacturer Phone2693246689
Manufacturer G1STRYKER CORP.
Manufacturer Street3800 E. CENTRE AVE.
Manufacturer CityPORTAGE MI 49002
Manufacturer CountryUS
Manufacturer Postal Code49002
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameSTAIR PRO - MODEL 6252
Generic NameSTAIR CHAIR
Product CodeIMK
Date Received2009-08-31
Model Number6252
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER CORP, MEDICAL DIVISION
Manufacturer AddressPORTAGE MI 49002 US 49002


Patients

Patient NumberTreatmentOutcomeDate
10 2009-08-31

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