MERIT CUSTOM KIT K12-MZT8231

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2019-10-15 for MERIT CUSTOM KIT K12-MZT8231 manufactured by Merit Medical Systems Inc..

Event Text Entries

[163047973] The suspect device has been returned for evaluation. A follow up will be submitted when the evaluation is complete.
Patient Sequence No: 1, Text Type: N, H10


[163048014] The distributor alleged that a foreign object was found inside the fluid path of the stopcock. This was identified during their initial inspection of received product. The device was not sent to a user facility.
Patient Sequence No: 1, Text Type: D, B5


[168930104] The suspect device has been returned for evaluation. The device was examined visually. The complaint is confirmed. No definitive root cause could be determined; however, it is attributed to the manufacturing process. A search of the complaint database was performed and no similar complaints for this lot number were found. The device history record was reviewed, and no exception documents were found.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1721504-2019-00088
MDR Report Key9194769
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2019-10-15
Date of Report2019-09-16
Date of Event2019-05-31
Date Mfgr Received2019-10-14
Device Manufacturer Date2019-02-07
Date Added to Maude2019-10-15
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 ContactMR. DAVID LOCKRIDGE
Manufacturer Street1600 MERIT PARKWAY
Manufacturer CitySOUTH JORDAN UT 84095
Manufacturer CountryUS
Manufacturer Postal84095
Manufacturer Phone8012084551
Manufacturer G1MERIT MEDICAL SYSTEMS INC.
Manufacturer Street1600 MERIT PARKWAY
Manufacturer CitySOUTH JORDAN, UT 84095
Manufacturer CountryUS
Manufacturer Postal Code84095
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMERIT CUSTOM KIT
Generic NameCUSTOM KIT
Product CodeOEQ
Date Received2019-10-15
Returned To Mfg2019-10-09
Catalog NumberK12-MZT8231
Lot NumberH1501706
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMERIT MEDICAL SYSTEMS INC.
Manufacturer Address1600 MERIT PARKWAY SOUTH JORDAN, UT 84095 US 84095


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-15

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