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 2011-02-15 for STAIR PRO - MODEL 6252 NA manufactured by Stryker Medical.

Event Text Entries

[18203893] Investigation underway.
Patient Sequence No: 1, Text Type: N, H10


[18375324] It was reported the tread did not function to specification. No pt involvement or adverse consequences have been reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1831750-2011-01404
MDR Report Key2022487
Report Source07
Date Received2011-02-15
Date of Report2011-01-18
Date of Event2011-01-17
Date Mfgr Received2011-01-18
Device Manufacturer Date2009-06-15
Date Added to Maude2011-04-07
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 Phone2693292100
Manufacturer G1STRYKER MEDICAL
Manufacturer Street3800 E. CENTRE AVE.
Manufacturer CityPORTAGE MI 49002
Manufacturer CountryUS
Manufacturer Postal Code49002
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTAIR PRO - MODEL 6252
Generic NameSTRETCHER, HAND-CARRIED
Product CodeIMK
Date Received2011-02-15
Model Number6252
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorOTHER
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER MEDICAL
Manufacturer AddressPORTAGE MI 49002 US 49002


Patients

Patient NumberTreatmentOutcomeDate
10 2011-02-15

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