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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ICU Medical Czech Republic a. s. Portex Tubes BLUselect Suctionaid; Tube, Tracheostomy (W/Wo Connector)

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ICU Medical Czech Republic a. s. Portex Tubes BLUselect Suctionaid; Tube, Tracheostomy (W/Wo Connector) Back to Search Results
Catalog Number 101/870/075CZ
Medical Device Problem Code Gas/Air Leak (2946)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/24/2026
Type of Reportable Event Malfunction
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Brand Name
Portex Tubes BLUselect Suctionaid
Common Device Name
Tube, Tracheostomy (W/Wo Connector)
Manufacturer (Section D)
ICU Medical Czech Republic a. s.
olomoucká 306
hranice NA 753 0 1
EZ  753 01
Manufacturer Contact
reed covert
951 calle amanecer
san clemente, CA 92673
+1(224)706-2300
MDR Report Key50892657
Report Number3011237704-2026-00013
Device Sequence Number10712616
Product Code BTO
UDI-Device Identifier15019517076219
UDI-Public(01)15019517076219(17)280816(10)4384992
Combination Product (Y/N)N
Initial Reporter StateNA
Initial Reporter CountryUK
PMA/510(K) Number
K173384
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Other,Foreign,User Facility
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 09/24/2026
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 Catalogue Number101/870/075CZ
Device Lot Number4384992
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 09/01/2026
Initial Report FDA Received Date09/25/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured09/19/2023
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexMale
Patient Weight165 LB
Patient RaceWhite
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