UNKNOWN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,foreign,health profe report with the FDA on 2018-02-24 for UNKNOWN manufactured by Alere San Diego, Inc..

Event Text Entries

[101149307] Investigation conclusion: it is indicated that the product is not returning for evaluation. As the customer did not provide a lot number, a manufacturing record review and testing on reserve sample from the same lot could not be performed. Further investigation is not possible at this time. Based on the information available, there is no indication of a product deficiency. A capa, capa-(b)(4), has been opened to address the late documentation of this complaint.
Patient Sequence No: 1, Text Type: N, H10


[101149308] The customer alleged receiving five instances of false positive cocaine results using an unspecified urine drug test. The patients admitted to using "bonsai drug" only. No additional information was provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2027969-2018-00023
MDR Report Key7294599
Report SourceCONSUMER,FOREIGN,HEALTH PROFE
Date Received2018-02-24
Date of Report2018-02-23
Date Mfgr Received2015-10-01
Date Added to Maude2018-02-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactYA-LING KING
Manufacturer Street9975 SUMMERS RIDGE ROAD
Manufacturer CitySAN DIEGO CA 92121
Manufacturer CountryUS
Manufacturer Postal92121
Manufacturer Phone8588052084
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN
Generic NameENZYME IMMUNOASSAY, COCAINE AND COCAINE METABOLITES
Product CodeDIO
Date Received2018-02-24
Model NumberUNKNOWN
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALERE SAN DIEGO, INC.
Manufacturer Address9975 SUMMERS RIDGE ROAD SAN DIEGO CA 92121 US 92121


Patients

Patient NumberTreatmentOutcomeDate
10 2018-02-24

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