HUDSON MULTI-ADAPTOR,15MM ID X 22MM OD 1422

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2017-05-26 for HUDSON MULTI-ADAPTOR,15MM ID X 22MM OD 1422 manufactured by Teleflex Medical.

Event Text Entries

[76077129] (b)(4). A visual inspection of the device involved in the complaint was performed on a picture provided by the customer. However this picture is not clear enough to confirm this customer complaint. A dimensional and functional inspection of the product involved in the complaint could not be conducted since the product was not returned at the time of this report. A device history record review shows that the product was assembled and inspected according to our specifications. Customer complaint cannot be confirmed based only on the information provided. Visual inspection of the product involved in the complaint was performed on a picture provided by the customer and it is not clear enough to confirm this customer complaint. To perform a proper investigation, and determine the source of the alleged defect reported, it is necessary to evaluate the sample involved in this complaint. However material from the production line was verified and no issues were found that can lead this customer complaint. If the device sample becomes available at a later date, this investigation will be updated with the evaluation results.
Patient Sequence No: 1, Text Type: N, H10


[76077130] Customer complaint alleges "believes they are having issues with carefusion or teleflex products depositing shards of plastic in the circuits". Alleged defect reported as detected during use. It was reported there was no patient injury or necessary medical intervention.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004365956-2017-00222
MDR Report Key6594271
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2017-05-26
Date of Report2017-05-16
Date of Event2017-05-16
Date Mfgr Received2017-08-24
Device Manufacturer Date2017-02-07
Date Added to Maude2017-05-26
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 ContactKATHARINE TARPLEY
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194334854
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetPARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHUDSON MULTI-ADAPTOR,15MM ID X 22MM OD
Generic NameCONNECTOR, AIRWAY
Product CodeBZA
Date Received2017-05-26
Returned To Mfg2017-08-04
Catalog Number1422
Lot Number74B1701012
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressRESEARCH TRIANGLE PARK NC


Patients

Patient NumberTreatmentOutcomeDate
10 2017-05-26

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