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

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 (b)(4) 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 and 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.The customer reports that this may be user error.

• 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: margie burton, rn ; 3015 carringtin mill blvd; morrisville, NC 27560 ; 9194334965
• MDR Report Key: 5914919
• MDR Text Key: 53501441
• Report Number: 3004365956-2016-00338
• Device Sequence Number: 1
• Product Code: BYX
• Combination Product (y/n): N
• Reporter Country Code: NZ
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 08/18/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/30/2016
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Device Expiration Date: 08/13/2020
• Device Catalogue Number: 1115
• Device Lot Number: 74H1501653
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 08/18/2016
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: OXYGEN CYLINDEROXYGEN FLOW METER