UNI-VENT, MODEL 731 799-EMBP-05-01

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-31 for UNI-VENT, MODEL 731 799-EMBP-05-01 manufactured by Zoll Medical Corporation.

Event Text Entries

[185797470] Zoll medical corporation has received the product and will be providing a supplemental report when our investigation is completed.
Patient Sequence No: 1, Text Type: N, H10


[185797471] Complainant alleged that while attempting to treat a patient (age & gender unknown), the device displayed an "unknown self check failure" error message. Complainant indicated that the clinician manually ventilated the patient to continue treatment. Complainant indicated that there was no adverse effect to the patient due to the reported malfunction.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1220908-2020-00800
MDR Report Key9904313
Date Received2020-03-31
Date of Report2020-03-10
Date of Event2020-03-09
Date Mfgr Received2020-03-10
Device Manufacturer Date2019-08-01
Date Added to Maude2020-03-31
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 Street269 MILL ROAD
Manufacturer CityCHELMSFORD MA 01824
Manufacturer CountryUS
Manufacturer Postal01824
Manufacturer Phone9784219552
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNI-VENT, MODEL 731
Generic NameVENTILATOR
Product CodeCBK
Date Received2020-03-31
Returned To Mfg2020-03-16
Model Number799-EMBP-05-01
Catalog Number799-EMBP-05-01
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerZOLL MEDICAL CORPORATION
Manufacturer Address269 MILL ROAD CHELMSFORD MA 01824 US 01824


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-31

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