MAUDE Adverse Event Report: COOK INC COOK AIRWAY EXCHANGE CATHETER; LRC CHANGER, TUBE, ENDOTRACHEAL

Model Number N/A

Device Problem Material Fragmentation (1261)

Patient Problem Foreign Body In Patient (2687)

Event Date 08/03/2017

Event Type  Injury  

Manufacturer Narrative

(b)(4).The event is currently under investigation.A follow-up report will be submitted upon receipt of additional information or completion of the investigation.

Event Description

It was reported by the international customer that, approximately one month following a procedure in which a cook airway exchange catheter was employed, the patient reported that they coughed up a piece of yellow tubing.The patient reported this issue during a scheduled, post-procedure medical checkup.The tube had reportedly been positioned for extubation during the original procedure, and was removed 15 minutes after the extubation was complete.The circumstances surrounding the usage and handling of the device are not fully known.The device is reportedly unavailable for return.

Manufacturer Narrative

Additional information: patient identifier.Corrected data: outcomes to adverse event.Investigation ¿ evaluation: a review of the complaint history, device history record, documentation, drawing, instructions for use (ifu), manufacturing instructions, specifications, and quality control of the device was conducted during the investigation.No issues were found related to the reported complaint.Complaint sample evaluation was not performed since no product or imaging was returned to assist with this investigation.Device, operating reports, photos, x-rays, and scans were requested, but were indicated as unavailable.The device history record for lot 8008132 was reviewed and noted one nonconformance that was reported within the manufacturing department.A review of the nonconformance data revealed that the nonconformance was recorded for "surface damaged¿ during the tipping process.These devices were scrapped and not replaced prior to further processing.Additionally, since the failure potentially involved a component device, the device history record for sa7874931 was reviewed and confirmed that no non-conformances were recorded.The manufacturing documents in place at the time of manufacture were reviewed and it was found that the device aspect in question was visually inspected by quality control and no notable gaps in production or processing controls were noted.Clinical assessment: the cook airway exchange catheter is used for replacement of endotracheal tubes whose inner diameter is 5mm or larger.It is intended for uncomplicated, atraumatic endotracheal tube exchange.There is no information regarding the type of endotracheal tube involved.According to the ifu, ¿ensure proper sizing of the cook airway exchange catheter within a double-lumen endotracheal tube.Failure to do so may cause small fragments to be shaved off during removal of the cook airway exchange catheter.¿ there is no information regarding any complications during the extubation that may have contributed to the piece of yellow tube.Per the ifu,catheters are stated to be used with endotracheal tubes whose inner diameter is 5 mm or larger.It is possible that the cook airway exchange catheter (c-cae-14.0-83) was used with an incompatible, undersized endotracheal tube which ultimately led to a portion of the catheter sheering off inside the patient and being left there.However, without visual, dimensional, or functional testing of the involved components, we are unable to determine with certainty what led to this failure mode.The failure could be attributed to user technique, product handling, human anatomy, device failure, or manufacturing-related causes.However, based on the information provided, no product returned, and the results of our investigation; a definitive root cause could not be determined.Per the quality engineering risk assessment, no further action is warranted.Monitoring will continue to be performed for similar complaints.

• Brand Name: COOK AIRWAY EXCHANGE CATHETER
• Type of Device: LRC CHANGER, TUBE, ENDOTRACHEAL
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• Manufacturer Contact: larry pool ; 750 daniels way; bloomington, IN 47404 ; 8128294891
• MDR Report Key: 6857375
• MDR Text Key: 85738568
• Report Number: 1820334-2017-02890
• Device Sequence Number: 1
• Product Code: LRC
• UDI-Device Identifier: 00827002078734
• UDI-Public: (01)00827002078734(17)200621(10)8008132
• Combination Product (y/n): N
• Reporter Country Code: IT
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional,u
• Reporter Occupation: Nurse
• Type of Report: Initial,Followup
• Report Date: 12/20/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/12/2017
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: C-CAE-14.0-83
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 12/14/2017
• Date Device Manufactured: 06/21/2017
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Life Threatening; Required Intervention