SHOE COVER, GRIPPER, NON-SKID * NON24758

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1999-09-30 for SHOE COVER, GRIPPER, NON-SKID * NON24758 manufactured by Medline Industries, Inc..

Event Text Entries

[183990] Reportedly two employees slipped wearing these shoe covers. No medical treatment was required.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1417592-1999-00031
MDR Report Key242755
Report Source06
Date Received1999-09-30
Date of Report1999-09-01
Date of Event1999-08-18
Date Reported to FDA1999-09-30
Date Reported to Mfgr1999-09-30
Date Added to Maude1999-10-05
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 Location3
Manufacturer ContactLARA SIMMONS
Manufacturer StreetONE MEDLINE PLACE
Manufacturer CityMUNDELEIN IL 60060
Manufacturer CountryUS
Manufacturer Postal60060
Manufacturer Phone8479492639
Manufacturer G1MEDLINE INDUSTRIES, INC.
Manufacturer StreetONE MEDLINE PLACE
Manufacturer CityMUNDELEIN IL 60060
Manufacturer CountryUS
Manufacturer Postal Code60060
Single Use3
Remedial ActionRC
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSHOE COVER, GRIPPER, NON-SKID
Generic NameSHOE COVER
Product CodeBWP
Date Received1999-09-30
Model Number*
Catalog NumberNON24758
Lot Number8320813JC3
ID Number*
OperatorOTHER
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key235184
ManufacturerMEDLINE INDUSTRIES, INC.
Manufacturer AddressONE MEDLINE PL. MUNDELEIN IL 60060 US
Baseline Brand NameSHOE COVER, GRIPPER, NON-SKID
Baseline Generic NameSHOE COVER
Baseline Model No*
Baseline Catalog NoNON24758
Baseline ID*
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1999-09-30

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