MERIT CUSTOM KIT K12-MZTS1201A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-11-02 for MERIT CUSTOM KIT K12-MZTS1201A manufactured by Merit Medical Systems, Inc..

Event Text Entries

[126110337] The suspect device is expected to return for evaluation. A follow up will be submitted when the evaluation is complete.
Patient Sequence No: 1, Text Type: N, H10


[126110338] The distributor alleged a defect in the packaging was found during initial inspection of received product. The device was not sent to a user facility.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1721504-2018-00118
MDR Report Key8034030
Date Received2018-11-02
Date of Report2018-10-10
Date of Event2018-08-16
Date Mfgr Received2018-12-10
Device Manufacturer Date2018-05-29
Date Added to Maude2018-11-02
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 ContactMRS. KATIE SWENSON, CQE, CBA, CQPA
Manufacturer Street1600 W MERIT PARKWAY
Manufacturer CitySOUTH JORDAN 84095
Manufacturer CountryUS
Manufacturer Postal84095
Manufacturer Phone8012081600
Manufacturer G1MERIT MEDICAL SYSTEMS, INC.
Manufacturer Street1600 W MERIT PARKWAY
Manufacturer CitySOUTH JORDAN 84095
Manufacturer CountryUS
Manufacturer Postal Code84095
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameMERIT CUSTOM KIT
Generic NameCUSTOM KIT
Product CodeOEQ
Date Received2018-11-02
Returned To Mfg2018-11-14
Catalog NumberK12-MZTS1201A
Lot NumberH1345689
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMERIT MEDICAL SYSTEMS, INC.
Manufacturer Address1600 W MERIT PARKWAY SOUTH JORDAN 84095 US 84095


Patients

Patient NumberTreatmentOutcomeDate
10 2018-11-02

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