HALYARD STERLING 50706

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-09-20 for HALYARD STERLING 50706 manufactured by Halyard Health, Inc..

Event Text Entries

[86756527]
Patient Sequence No: 1, Text Type: N, H10


[86756528] Halyard sterling nitrile powder free exam gloves, size small, ref 50706 have visible 'weak' areas on one or more fingers of the gloves. Not every glove is affected although a majority of random gloves throughout the box have these 'weak' areas and several create holes or tear as user is inserting hand into the glove. Currently have (2) boxes of this same lot affected. Currently no issues reported with the other sizes of halyard gloves.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6878539
MDR Report Key6878539
Date Received2017-09-20
Date of Report2017-09-07
Date of Event2017-08-29
Report Date2017-09-07
Date Reported to FDA2017-09-07
Date Reported to Mfgr2017-09-07
Date Added to Maude2017-09-20
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHALYARD STERLING
Generic NameSPECIALTY -TESTED FOR USE WITH CHEMOTHERAPY - PATIENT EXAMINATION GLOVE
Product CodeLZC
Date Received2017-09-20
Catalog Number50706
Lot NumberSP7143ZZZ_08AX
OperatorNURSE
Device Availability*
Device Age4 MO
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHALYARD HEALTH, INC.
Manufacturer Address5405 WINDWARD PARKWAY ALPHARETTA GA 30004 US 30004


Patients

Patient NumberTreatmentOutcomeDate
10 2017-09-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.