HENRY SCHEIN HCG URINE CASSETTE 100T FHC-102

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-24 for HENRY SCHEIN HCG URINE CASSETTE 100T FHC-102 manufactured by Alere San Diego.

Event Text Entries

[188824645] Results pending completion of the investigation.
Patient Sequence No: 1, Text Type: N, H10


[188824646] A customer working at a clinic reported two false positives occurring on (b)(6) 2020 with hcg urine cassettes. The laboratory beta quant result taken the same day was <1 iu/ml. There was no report of an adverse event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2027969-2020-00015
MDR Report Key9874284
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-03-24
Date of Report2020-03-24
Date of Event2020-03-09
Date Mfgr Received2020-03-10
Date Added to Maude2020-03-24
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 ContactMONIKA BURRELL
Manufacturer Street9975 SUMMERS RIDGE ROAD
Manufacturer CitySAN DIEGO, CA
Manufacturer CountryUS
Manufacturer Phone8052506
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHENRY SCHEIN HCG URINE CASSETTE 100T
Generic NameHCG PREGNANCY TEST`
Product CodeJHI
Date Received2020-03-24
Model NumberFHC-102
Lot NumberHCG9092050
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerALERE SAN DIEGO
Manufacturer Address9975 SUMMERS RIDGE RD SAN DIEGO, CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-24

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