Q2 IV EXTENSION SET 95906

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-18 for Q2 IV EXTENSION SET 95906 manufactured by Quest Medical, Inc.

Event Text Entries

[142538270] The complaint sample was not returned for investigation and no lot number was provided. A dhr review could not be conducted without the lot number. A similar product was pulled from quest's inventory and the samples were tested. The reported complaint condition of media shooting outside the tubing could not duplicated. The root cause of the reported complaint is unknown. A possible root cause may be improper clamping of the tubing by the end user. Quest will continue to monitor trends for the reported complaint condition.
Patient Sequence No: 1, Text Type: N, H10


[142538271] The report received states that the clamps on the extension sets do not hold tightly and causes contrast dye to shoot out side tubing. Multiple patients have had to receive double doses of contrast media to complete studies and other means of clamping the tubing have had to be used to prevent the issue from happening. There were no reported patient complications resulting from the alleged issue.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1649914-2019-00022
MDR Report Key8529088
Date Received2019-04-18
Date of Report2019-04-18
Date Mfgr Received2019-03-20
Date Added to Maude2019-04-18
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 NameQ2 IV EXTENSION SET
Generic NameIV EXTENSION SETS
Product CodeFPK
Date Received2019-04-18
Model Number95906
Device AvailabilityN
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
101. Required No Informationntervention 2019-04-18

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