DURAFIT SHOECOVER, ANTISKID 4852

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1999-11-12 for DURAFIT SHOECOVER, ANTISKID 4852 manufactured by Allegiance Healthcare Corp.

Event Text Entries

[184394] It has been reported that an employee working in the operating room slipped and fell while wearing the shoe covers for approx 4 hours. Employee was sent the occupational health resource center at the hosp to be checked out. No medical treatment was required. Employee was released back to work on lite duty.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1423507-1999-00330
MDR Report Key249982
Report Source05
Date Received1999-11-12
Date of Report1999-11-12
Date of Event1999-10-19
Date Mfgr Received1999-10-25
Date Added to Maude1999-11-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactMICHELE DONATICH
Manufacturer Street1500 WAUKEGAN RD
Manufacturer CityMCGAW PARK IL 60085
Manufacturer CountryUS
Manufacturer Postal60085
Manufacturer Phone8477853309
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDURAFIT SHOECOVER, ANTISKID
Generic NameDURAFIT SHOECOVER, ANTISKID
Product CodeFXP
Date Received1999-11-12
Returned To Mfg1999-11-08
Model Number4852
Catalog Number4852
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key242190
ManufacturerALLEGIANCE HEALTHCARE CORP
Manufacturer Address1500 WAUKEGAN RD MCGAW PARK IL 60085 US
Baseline Brand NameDURAFIT SHOECOVER, ANTISKID
Baseline Generic NameDURAFIT SHOECOVER
Baseline Model No4852
Baseline Catalog No4852
Baseline IDNA
Baseline Device FamilyAPPAREL
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK800528
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1999-11-12

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