LIQUICHEK IMMUNCASSAY PLUS CONTROL * 360

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,05 report with the FDA on 2001-12-20 for LIQUICHEK IMMUNCASSAY PLUS CONTROL * 360 manufactured by Bio-rad Laboratories.

Event Text Entries

[243252] A laboratory technician cut their finger on a metal crimp when attempting to open a control vial.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2016706-2001-00006
MDR Report Key369009
Report Source04,05
Date Received2001-12-20
Date of Report2001-12-19
Date of Event2001-10-24
Date Mfgr Received2001-11-15
Device Manufacturer Date2001-04-01
Date Added to Maude2002-01-03
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 ContactYVETTE LLOYD
Manufacturer Street9500 JERONIMO ROAD
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9495981465
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 NameLIQUICHEK IMMUNCASSAY PLUS CONTROL
Generic NameQUALITY CONTROL MATERIAL
Product CodeJJT
Date Received2001-12-20
Model Number*
Catalog Number360
Lot Number40590
ID Number*
Device Expiration Date2003-05-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key358124
ManufacturerBIO-RAD LABORATORIES
Manufacturer Address9500 JERONIMO RD. IRVINE CA 92618 US
Baseline Brand NameLIQUICHEK IMMUNCASSAY PLUS CONTROL
Baseline Generic NameQUALITY CONTROL MATERIAL
Baseline Model No*
Baseline Catalog No360
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2001-12-20

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