MICRO-TOUCH LATEX MEDICAL GLOVES UNK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00 report with the FDA on 2000-01-26 for MICRO-TOUCH LATEX MEDICAL GLOVES UNK manufactured by Johnson & Johnson Medical, Mfg. Sdn.bhd.

Event Text Entries

[17807612] Plaintiff was employed as a registered nurse who wore and was exposed to latex gloves made by various manufacturers. Plaintiff alleges developing a latex allergy.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1618732-2000-00014
MDR Report Key259975
Report Source00
Date Received2000-01-26
Date of Report2000-01-21
Date Mfgr Received2000-01-21
Date Added to Maude2000-01-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationATTORNEY
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactMARGARET MARSH, MGR
Manufacturer Street2500 ARBROOK BLVD
Manufacturer CityARLINGTON TX 760143899
Manufacturer CountryUS
Manufacturer Postal760143899
Manufacturer Phone8004235850
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameMICRO-TOUCH LATEX MEDICAL GLOVES
Generic NameGLOVES, MEDICAL, LATEX
Product CodeLYX
Date Received2000-01-26
Model NumberNA
Catalog NumberUNK
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key251774
ManufacturerJOHNSON & JOHNSON MEDICAL, MFG. SDN.BHD
Manufacturer AddressPERSIARAN PERUSAHAAN SECTION 23, LOT 16, SHAH ALAM SELANGOR DARUL EHSAN MY 40000


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2000-01-26

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