SADDLELOOP 18GX10CM WITH BLUNT NEEDLE 1541

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-04-05 for SADDLELOOP 18GX10CM WITH BLUNT NEEDLE 1541 manufactured by Quest Medical, Inc..

Event Text Entries

[72175315] The international distributor ((b)(4)) reported an issue encountered with the saddleloop device during use. The clinician reported that the tensioner came off the tubing. The report stated another package of the same device was used instead to complete the procedure. There were no patient complications reported as a result of the alleged issue. The device was discarded and not returned to the distributor or manufacturer for evaluation.
Patient Sequence No: 1, Text Type: D, B5


[74296664] The device was not returned for evaluation. A possible root cause of the reported issue would be insufficient adhesive used; however, this could not be confirmed with no devices returned. The device history record for the lot was reviewed and no devices were rejected and no specific manufacturing yield issues were reported similar to the reported complaint condition
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1649914-2017-00032
MDR Report Key6460328
Date Received2017-04-05
Date of Report2017-04-25
Date of Event2017-03-02
Date Mfgr Received2017-03-15
Device Manufacturer Date2015-11-12
Date Added to Maude2017-04-05
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. AMY CLENDENING-WHEELER
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 Report3

Device Details

Brand NameSADDLELOOP 18GX10CM WITH BLUNT NEEDLE
Generic NameVASCULAR LOOP
Product CodeGAE
Date Received2017-04-05
Model Number1541
Lot Number0501965N05
Device Expiration Date2019-11-11
OperatorPHYSICIAN
Device AvailabilityN
Device AgeDA
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 2017-04-05

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