MERIT CUSTOM KIT K04-MK2100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-29 for MERIT CUSTOM KIT K04-MK2100 manufactured by Merit Medical Systems.

Event Text Entries

[143680307] 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


[143680309] The distributor reported a defect in the packaging. 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


MAUDE Entry Details

Report Number3011642792-2019-00007
MDR Report Key8562690
Date Received2019-04-29
Date of Report2019-04-02
Date of Event2019-03-22
Date Mfgr Received2019-06-18
Device Manufacturer Date2019-01-30
Date Added to Maude2019-04-29
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 MERIT PARKWAY
Manufacturer CitySOUTH JORDAN UT 84095
Manufacturer CountryUS
Manufacturer Postal84095
Manufacturer Phone8012531600
Manufacturer G1MERIT MEDICAL SYSTEMS
Manufacturer Street8830 SIEMPRE VIVA RD #100
Manufacturer CitySAN DIEGO CA 92154
Manufacturer CountryUS
Manufacturer Postal Code92154
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameMERIT CUSTOM KIT
Generic NameCUSTOM KIT
Product CodeOJA
Date Received2019-04-29
Returned To Mfg2019-04-15
Catalog NumberK04-MK2100
Lot NumberI1508802
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMERIT MEDICAL SYSTEMS
Manufacturer Address8830 SIEMPRE VIVA RD #100 SAN DIEGO CA 92154 US 92154


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-29

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