MAUDE Adverse Event Report: COVIDIEN ENTRFLX 10FR;43IN W/ STYLETCN; TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Model Number	721088CN
Medical Device Problem Code	Difficult to Remove (1528)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	07/08/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The complainant indicated that the device will not be returned for evaluation; therefore, a failure analysis is not available, and we are not able to determine the relationship between this device and the cause for this event.If additional information or the sample is received, the investigation will be reopened and responded to accordingly.
Event or Problem Description
The customer reported the patient was admitted from the emergency department (ed) and when they arrived to the intensive care unit, the guide wire wouldn¿t come out of the tube.There was no harm to the patient.

• Brand Name: ENTRFLX 10FR;43IN W/ STYLETCN
• Common Device Name: TUBES, GASTROINTESTINAL (AND ACCESSORIES)
• Manufacturer (Section D): COVIDIEN; 15 hampshire street; mansfield MA 02048
• MDR Report Key: 10313580
• Report Number: 1282497-2020-09214
• Device Sequence Number: 3376635
• Product Code: KNT
• UDI-Device Identifier: 20884521033617
• UDI-Public: 20884521033617
• Combination Product (Y/N): N
• Initial Reporter State: AL
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,user f
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 07/23/2020

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: 721088CN
• Device Catalogue Number: 721088CN
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 07/09/2020
• Initial Report FDA Received Date: 07/23/2020
• Patient Sequence Number: 1