CRUTCH, FOREARM MDS805160 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,07 report with the FDA on 2004-09-24 for CRUTCH, FOREARM MDS805160 * manufactured by Medline Industries, Inc..

Event Text Entries

[329499] Reportedly an end user fell when the cuff broke on a forearm crutch, and bruised their ribs and sprained their shoulder.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1417592-2004-00027
MDR Report Key546748
Report Source04,07
Date Received2004-09-24
Date of Report2004-09-24
Date of Event2004-08-30
Date Mfgr Received2004-08-30
Device Manufacturer Date2001-11-01
Date Added to Maude2004-10-04
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 Location0
Manufacturer ContactANDREA HAFERKAMP
Manufacturer StreetONE MEDLINE PLACE
Manufacturer CityMUNDELEIN IL 60060
Manufacturer CountryUS
Manufacturer Postal60060
Manufacturer Phone8478372759
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCRUTCH, FOREARM
Generic NameCRUTCH
Product CodeIRP
Date Received2004-09-24
Model NumberMDS805160
Catalog Number*
Lot Number*
ID Number*
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key536156
ManufacturerMEDLINE INDUSTRIES, INC.
Manufacturer AddressONE MEDLINE PL. MUNDELEIN IL 60060 US
Baseline Brand NameCRUTCH, FORMEARM ALUMINUMTALL A
Baseline Generic NameCRUTCH
Baseline Model NoMDS805160
Baseline Catalog No*
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2004-09-24

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