SHOECOVER PREMIUM ANTISKID 5852

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2004-12-17 for SHOECOVER PREMIUM ANTISKID 5852 manufactured by Cardinal Health.

Event Text Entries

[314180] Staff member in pharmacy fell due to slipperiness of shoe cover.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1423507-2004-00131
MDR Report Key560316
Report Source05,07
Date Received2004-12-17
Date of Report2004-12-17
Date Mfgr Received2004-11-18
Device Manufacturer Date2001-10-01
Date Added to Maude2004-12-21
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 ContactMICHELE DONATICH, DIRECTOR
Manufacturer Street1430 WAUKEGAN ROAD BLDG KB
Manufacturer CityMCGAW PARK IL 60085
Manufacturer CountryUS
Manufacturer Postal60085
Manufacturer Phone8475786412
Manufacturer G11623223-SURGICAL GROUP EL PASO
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSHOECOVER PREMIUM ANTISKID
Generic NameSHOECOVER PREMIUM ANTISKID
Product CodeFXP
Date Received2004-12-17
Model Number5852
Catalog Number5852
Lot Number03HAK2378
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key550009
ManufacturerCARDINAL HEALTH
Manufacturer Address* MCGAW PARK IL * US
Baseline Brand NameSHOECOVER PREMIUM ANTISKID
Baseline Generic NameSHOECOVER PREMIUM ANTISKID
Baseline Model No5852
Baseline Catalog No5852
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2004-12-17

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