MAUDE Adverse Event Report: COVIDIEN DOBBHOFF 8FR;43IN W/ STYLETCN; TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Model Number	710859CN
Medical Device Problem Code	Difficult to Remove (1528)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The incident sample has been requested but to date has not been received for evaluation.  if the sample is received, or if additional information pertinent to the incident is obtained a follow-up report will be submitted.  as part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.
Event or Problem Description
The customer reported the stylet would not come out of the ng tube.

• Brand Name: DOBBHOFF 8FR;43IN W/ STYLETCN
• Common Device Name: TUBES, GASTROINTESTINAL (AND ACCESSORIES)
• Manufacturer (Section D): COVIDIEN; 15 hampshire street; mansfield MA 02048
• MDR Report Key: 8961036
• Report Number: 1282497-2019-08636
• Device Sequence Number: 2471334
• Product Code: KNT
• UDI-Device Identifier: 10884521146112
• UDI-Public: 10884521146112
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,other,use
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 09/04/2019

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: Health Professional
• Device Model Number: 710859CN
• Device Catalogue Number: 710859CN
• Device Lot Number: 191580141
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 09/03/2019
• Initial Report FDA Received Date: 09/04/2019
• Patient Sequence Number: 1