SHOE COVER, GRIPPER * NON23758

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 1999-08-24 for SHOE COVER, GRIPPER * NON23758 manufactured by Medline Industries, Inc..

Event Text Entries

[19958611] Reportedly, personnel have slipped while wearing shoe covers, one nurse broke a finger and required stitches.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1417592-1999-00024
MDR Report Key237138
Report Source06
Date Received1999-08-24
Date of Report1999-07-21
Date of Event1999-07-19
Date Reported to FDA1999-10-15
Date Reported to Mfgr1999-10-15
Date Added to Maude1999-08-27
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
Generic NameSHOE COVER
Product CodeFXP
Date Received1999-08-24
Model Number*
Catalog NumberNON23758
Lot Number9393372JC1
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key229807
ManufacturerMEDLINE INDUSTRIES, INC.
Manufacturer AddressONE MEDLINE PLACE MUNDELEIN IL 60060 US
Baseline Brand NameSHOE COVER, GRIPPER, NON-SKID
Baseline Generic NameSHOE COVER
Baseline Model NoNON23758
Baseline Device FamilyDI01
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1999-08-24

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