MAUDE Adverse Event Report: TELEFLEX MEDICAL LMA FASTRACH COMBO-KIT, SU, SIZE 5; LMA FASTRACH (SU)

Model Number	IPN042410
Medical Device Problem Code	Difficult to Insert (1316)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/07/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).
Event or Problem Description
It was reported "experiencing difficulty inserting et tubes into lma fastrachs.The et tubes are always lubricated, but still tend to get hung up on something inside of the lma fastrachs".No patient involvement reported.
Event or Problem Description
It was reported "experiencing difficulty inserting et tubes into lma fastrachs.The et tubes are always lubricated, but still tend to get hung up on something inside of the lma fastrachs".No patient involvement reported.
Additional Manufacturer Narrative
(b)(4).Complaint verification testing could not be performed as it was reported that the sample is not available for return.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.

• Brand Name: LMA FASTRACH COMBO-KIT, SU, SIZE 5
• Common Device Name: LMA FASTRACH (SU)
• Manufacturer (Section D): TELEFLEX MEDICAL; athlone
• MDR Report Key: 11235973
• Report Number: 3004365956-2021-00023
• Device Sequence Number: 19693716
• Product Code: CAE
• UDI-Device Identifier: 05060112311888
• UDI-Public: 05060112311888
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K051993
• 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,Followup
• Report Date (Section B): 01/07/2021

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: IPN042410
• Device Catalogue Number: 135250
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 01/07/2021
• Supplement Date Received by Manufacturer: 02/11/2021
• Initial Report FDA Received Date: 01/27/2021
• Supplement Report FDA Received Date: 02/12/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: N/A.