LIQUICHEK LIPIDS CONTROL ,LEVEL 2 642

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-09-21 for LIQUICHEK LIPIDS CONTROL ,LEVEL 2 642 manufactured by Bio-rad Laboratories Inc.

Event Text Entries

[121469073] The labeling for liquichek lipids,control indicates this product manufactured from human source material components and contains a warning statement and a caution symbol indicating the product contains human source material and must be treated as potentially infectious. Each human donor unit used to manufacture this product was tested as required by fda accepted methods. Tests results were non-reactive or negative for evidence of infection due to human immunodeficiency virus (hiv), hepatitis b virus (hbv) and hepatitis c virus (hcv). This product may also contain other human source materials for which there are no approved tests. In accordance with good laboratory practice, all human source material should be considered potentially infectious and handled with the same precautions used with patient specimens.
Patient Sequence No: 1, Text Type: N, H10


[121469074] On (b)(6) a physician assistant called to report that she had a patient seeking treatment. The patient splashed liquichek lipids control, lot 57542, into her right eye and on her left cheek. The user was not wearing laboratory goggles but was wearing regular eyeglasses. Physician assistant irrigated her eye with saline.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2016706-2018-00003
MDR Report Key7899083
Report SourceHEALTH PROFESSIONAL
Date Received2018-09-21
Date of Report2018-09-10
Date of Event2018-08-23
Date Mfgr Received2018-08-23
Device Manufacturer Date2016-04-30
Date Added to Maude2018-09-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS MARIA ZEBALLOS
Manufacturer Street9500 JERONIMO ROAD
Manufacturer CityIRVINE 926182017
Manufacturer CountryUS
Manufacturer Postal926182017
Manufacturer Phone9495981220
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLIQUICHEK LIPIDS CONTROL ,LEVEL 2
Generic NameMULTI-ANALYTE CONTROL,ALL KINDS (ASSAYED) PRODUCT CODE :JJY
Product CodeJJY
Date Received2018-09-21
Catalog Number642
Lot Number57542
Device Expiration Date2019-04-30
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBIO-RAD LABORATORIES INC
Manufacturer Address9500 JERONIMO ROAD IRVINE CA 926182017 US 926182017


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-09-21

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