RETROGUARD ARTERIAL SAFETY VALVE 4007100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-05-04 for RETROGUARD ARTERIAL SAFETY VALVE 4007100 manufactured by Quest Medical, Inc.

Event Text Entries

[108001375] The alleged incident occurred outside of the us. This medwatch is being submitted because quest manufactures a similar device in the us. As of date the lot number of the device with the alleged defect has not been provided by the customer and it is unknown if the product was used on a patient. An investigation will be conducted and a follow medwatch will be submitted if additional information becomes available.
Patient Sequence No: 1, Text Type: N, H10


[108001376] A report was received regarding an alleged issue with the valve. The report states that particulate matter which looks like metallic fragment was found in the housing of the valve.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1649914-2018-00044
MDR Report Key7489000
Date Received2018-05-04
Date of Report2018-05-04
Date Mfgr Received2018-04-11
Date Added to Maude2018-05-04
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 ContactTOSAN ONOSODE
Manufacturer StreetONE ALLENTOWN PARKWAY
Manufacturer CityALLEN TX 75002
Manufacturer CountryUS
Manufacturer Postal75002
Manufacturer Phone9723326338
Manufacturer G1QUEST MEDICAL, INC
Manufacturer StreetONE ALLENTOWN PARKWAY
Manufacturer CityALLEN TX 75002
Manufacturer CountryUS
Manufacturer Postal Code75002
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameRETROGUARD ARTERIAL SAFETY VALVE
Generic NameCPB CHECK VALVE
Product CodeMJJ
Date Received2018-05-04
Returned To Mfg2018-04-24
Model Number4007100
Catalog Number4007100
Device AvailabilityR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerQUEST MEDICAL, INC
Manufacturer AddressONE ALLENTOWN PARKWAY ALLEN TX 75002 US 75002


Patients

Patient NumberTreatmentOutcomeDate
10 2018-05-04

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