MAUDE Adverse Event Report: CARDINAL HEALTH ENTRFLX 10FR 43IN W STY YPORT; TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Model Number	8884721088E
Medical Device Problem Code	Material Separation (1562)
Health Effect - Clinical Code	Foreign Body In Patient (2687)
Date of Event	04/19/2024
Type of Reportable Event	Serious Injury
Event or Problem Description
Per customer, the gastrointestinal (gi) reported that the kf tube have had removed via scope.The tube was inserted on april 10th.It was identified as a problem and the proximal piece removed on april 19th.The distal piece was removed via scope on april 20th.In addition to an unnecessary procedure, the patient also went approximately 24 hours without feeds and missed medications.Additional information was received from the customer and stated that the tube burst into two pieces.The split occurred in the middle of the tube not at the weight or y-port.The weight was still attached.The distal piece refers to the piece of the tube that was remaining in the patient and the weighted tip was attached to this piece.The distal piece was removed via endoscopy procedure.The staff further stated that they think the tubes that are breaking are more pliable than normal and seem to be softer.
Additional Manufacturer Narrative
An investigation is currently underway.Upon completion, the results will be forwarded.
Additional Manufacturer Narrative
Since a lot number was not provided, the device history record review could not be performed.As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.One sample was received for the evaluation.The sample arrived was widely used with a dark color, it was observed that in 1 part of the tube a kind of balloon was inflated, and in that part the tube broke, the other missing part of the tube was not received for analysis.The reported condition was confirmed; however, the condition was not confirmed as originating at the manufacturing site.A walk through of the manufacturing process was performed showing all process and controls were found properly followed.The definitive root cause of the reported issue could not be determined.This complaint will be used for tracking and trending purposes.

• Brand Name: ENTRFLX 10FR 43IN W STY YPORT
• Common Device Name: TUBES, GASTROINTESTINAL (AND ACCESSORIES)
• Manufacturer (Section D): CARDINAL HEALTH; 777 west street; mansfield MA 02048
• Manufacturer (Section G): CARDINAL HEALTH; calle 9 sur no. 125 cuidad ind; tijuana 22500 ; MX 22500
• Manufacturer Contact: jill saraiva ; 777 west street; mansfield, MA 02048 ; 5086183640
• MDR Report Key: 19261945
• Report Number: 9612030-2024-00063
• Device Sequence Number: 2581954
• Product Code: KNT
• UDI-Device Identifier: 10884521582996
• UDI-Public: 10884521582996
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 08/01/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Model Number: 8884721088E
• Device Catalogue Number: 8884721088E
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/24/2024
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/07/2024
• Supplement Report FDA Received Date: 08/01/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: A
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown