NARA, DOMESTIC 4402 4402000001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-01-28 for NARA, DOMESTIC 4402 4402000001 manufactured by Stryker Medical-kalamazoo.

Event Text Entries

[176868238] This mdr is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program. The device is pending evaluation. There was no remedial action taken. This device is not labeled for single use.
Patient Sequence No: 1, Text Type: N, H10


[176868239] This report summarizes 1 malfunction event, where it was reported the gap on the side of the mattress was too big. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001831750-2020-00281
MDR Report Key9638813
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-01-28
Date of Report2020-01-28
Date of Event2020-01-01
Date Mfgr Received2020-01-01
Date Added to Maude2020-01-28
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. KRISTEN CANTER
Manufacturer Street3800 EAST CENTRE AVENUE
Manufacturer CityPORTAGE MI 49002
Manufacturer CountryUS
Manufacturer Postal49002
Manufacturer Phone2693292100
Manufacturer G1STRYKER MEDICAL-KALAMAZOO
Manufacturer Street3800 EAST CENTRE AVENUE
Manufacturer CityPORTAGE MI 49002
Manufacturer CountryUS
Manufacturer Postal Code49002
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNARA, DOMESTIC
Generic NameBASSINET, HOSPITAL
Product CodeNZG
Date Received2020-01-28
Model Number4402
Catalog Number4402000001
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER MEDICAL-KALAMAZOO
Manufacturer Address3800 EAST CENTRE AVENUE PORTAGE MI 49002 US 49002


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-28

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