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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: TELEFLEX MEDICAL HUDSON TUBING, OXYGEN SUPPLY 7'; PRESSURE TUBING & ACCESSORIES

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TELEFLEX MEDICAL HUDSON TUBING, OXYGEN SUPPLY 7'; PRESSURE TUBING & ACCESSORIES Back to Search Results
Catalog Number 1115
Device Problem Kinked (1339)
Patient Problems No Known Impact Or Consequence To Patient (2692); No Information (3190)
Event Date 08/15/2016
Event Type  malfunction  
Manufacturer Narrative
(b)(4).It is unknown if the device sample is available for evaluation.A visual, functional, and dimensional inspection of the product involved in the complaint could not be conducted since the product was not returned.No picture available for review.The device history record of batch number 74l1501103 that belong to catalog number 1115 has been reviewed and no issues or discrepancies were found which could potentially be related to this complaint.No non conformance reports were originated for the lot in question that can be associated to the complaint reported.Dhr shows that the product was assembled & inspected according to our specifications.Customer complaint cannot be confirmed based only on the information provided, to perform an investigation and determine the source of defect reported it is necessary to evaluate the sample involved in this customer complaint.However material from the production line was inspected and no issues were detected that can lead this customer complaint.If the device sample becomes available at a later date this complaint will be re-opened.
 
Event Description
The customer alleges that the oxygen tubing kinks and occludes and prevents the delivery of oxygen to the patient.The kink/occlusion is at the point of attachment.The customer, also, indicates that the tubing is connected to an oxygen cylinder or flow meter and when pulled tightly there is kinking.
 
Manufacturer Narrative
(b)(4).The sample was returned for evaluation.A visual exam was performed and no kinked tubing was observed.Based on the visual exam, the reported complaint could not be confirmed.There were no issues found with the returned sample.
 
Event Description
The customer alleges that the oxygen tubing kinks and occludes and prevents the delivery of oxygen to the patient.The kink/occlusion is at the point of attachment.The customer, also, indicates that the tubing is connected to an oxygen cylinder or flow meter and when pulled tightly there is kinking.
 
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Brand Name
HUDSON TUBING, OXYGEN SUPPLY 7'
Type of Device
PRESSURE TUBING & ACCESSORIES
Manufacturer (Section D)
TELEFLEX MEDICAL
research triangle park NC
Manufacturer (Section G)
TELEFLEX MEDICAL
parque industrial finsa
nuevo laredo 88275
MX   88275
Manufacturer Contact
katharine tarpley
3015 carrington mill blvd
morrisville, NC 27560
9194334854
MDR Report Key5915425
MDR Text Key53513520
Report Number3004365956-2016-00341
Device Sequence Number1
Product Code BYX
Combination Product (y/n)N
Reporter Country CodeNZ
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type foreign,health professional,u
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 08/18/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/30/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator No Information
Device Expiration Date11/13/2020
Device Catalogue Number1115
Device Lot Number74L1501103
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer06/29/2017
Is the Reporter a Health Professional? Yes
Date Manufacturer Received07/24/2017
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured11/10/2015
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Treatment
OXYGEN CYLINDEROXYGEN FLOW METER
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