MAUDE Adverse Event Report: BARD ACCESS SYSTEMS JEJUNAL FEEDING TUBE 9F; JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES

Model Number	000319
Medical Device Problem Code	Material Frayed (1262)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
As the lot number for the device was provided, a manufacturing review will be performed.The sample was not returned to the manufacturer for inspection/evaluation.Therefore, the investigation of the reported event is inconclusive.Based upon the available information, the definitive root cause for this event is unknown.The instructions for use (ifu) is adequate for the reported device/patient code(s) and provides general instructions for use, as well as warnings, precautions and potential complications associated with the device.Upon receipt of new or additional information, a follow-up report will be submitted as applicable.
Event or Problem Description
This report summarizes one malfunction.A review of the reported information indicated that model 000319.Jejunal feeding/gastric decompression tubes allegedly experienced material frayed.This report was received from a single source.This event did involve patient with no reported patient injury.The patient is (b)(6); however, weight and gender was not provided.

• Brand Name: JEJUNAL FEEDING TUBE 9F
• Common Device Name: JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES
• Manufacturer (Section D): BARD ACCESS SYSTEMS; 605 n. 5600 w.; salt lake city UT 84116
• MDR Report Key: 8796449
• Report Number: 3006260740-2019-01971
• Device Sequence Number: 2540624
• Product Code: KNT
• UDI-Device Identifier: 00801741051630
• UDI-Public: (01)00801741051630
• Combination Product (Y/N): N
• Initial Reporter State: AZ
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 07/16/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: No Information
• Device Model Number: 000319
• Device Catalogue Number: 000319
• Device Lot Number: ASCZF007
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/30/2019
• Initial Report FDA Received Date: 07/16/2019
• Patient Sequence Number: 1