MAUDE Adverse Event Report: AMBU A/S AMBU VIVASIGHT 2 DLT; DOUBLE-LUMEN ENDOBRONCHIAL TUBE

Model Number	412371000
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/10/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The vivasight2 dlt kit 37 fr-left were not returned for investigation due to contamination.However, the user provided pictures to assist investigation.Based on the pictures provided it was observed that the tracheal cuff was damaged.Prior to procedure the affected products had undergone cuff integrity check in accordance with instructions for use.The tracheal cuffs were able to inflate without any leakage observed.The two affected lots manufacturing history showed no similar failures for the affected lot#1000580965, while for the other affected lot#1000597243 one piece was rejected due to a similar reported failure (tracheal cuff and pilot balloon not able to inflate).The affected lot has been re-screened and no similar failures were detected.Further investigation was performed on samples with the same manufacturing lots.The tracheal cuff functionality was checked on the retention samples.The tracheal cuff was inflated, and no leakage was observed.
Event or Problem Description
During procedure with vivasight 2 dlt the tracheal cuff broke inside the patient.The tube was replaced with a second tube.After around one hour the patient had to be re-intubated with a third tube to gain control of the airway during the procedure.It was confirmed that there was no harm to the patient and no impact on patient outcome.Two replacements and a total of three dlt tubes are required to gain control of the airway during the operation.

• Brand Name: AMBU VIVASIGHT 2 DLT
• Common Device Name: DOUBLE-LUMEN ENDOBRONCHIAL TUBE
• Manufacturer (Section D): AMBU A/S; baltorpbakken 13; ballerup, denmark 2750, ; DA 2750,
• MDR Report Key: 13737567
• Report Number: 1220828-2022-00005
• Device Sequence Number: 12004755
• Product Code: CBI
• UDI-Device Identifier: 05707480145737
• UDI-Public: 05707480145737
• Combination Product (Y/N): N
• Initial Reporter Country: SW
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Importer
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 03/11/2022

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: 412371000
• Device Catalogue Number: 412371000
• Device Lot Number: 1000597243, 100580965
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 02/11/2022
• Event Location: Hospital
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 03/11/2022
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown