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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ICU Medical Healthcare Manufacturing S.A. de C.V. Portex BLUSelect Tracheostomy Tube; Tube, Tracheostomy (W/Wo Connector)

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ICU Medical Healthcare Manufacturing S.A. de C.V. Portex BLUSelect Tracheostomy Tube; Tube, Tracheostomy (W/Wo Connector) Back to Search Results
Catalog Number 101/870/090
Medical Device Problem Code Crack (1135)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/01/2026
Type of Reportable Event Malfunction
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Brand Name
Portex BLUSelect Tracheostomy Tube
Common Device Name
Tube, Tracheostomy (W/Wo Connector)
Manufacturer (Section D)
ICU Medical Healthcare Manufacturing S.A. de C.V.
avenida calidad no.4, parque
tijuana NA 22425
MX  22425
Manufacturer Contact
reed covert
951 calle amanecer
san clemente, CA 92673
+1(224)706-2300
MDR Report Key50811293
Report Number9617604-2026-00815
Device Sequence Number20968218
Product Code BTO
UDI-Device Identifier15019517078022
UDI-Public(01)15019517078022
Combination Product (Y/N)N
Initial Reporter StateNA
Initial Reporter CountryUK
PMA/510(K) Number
Unknown
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,User Facility
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 09/17/2026
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 Other
Device Catalogue Number101/870/090
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer09/14/2026
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/25/2026
Initial Report FDA Received Date09/17/2026
Was Device Evaluated by Manufacturer? (Y/N) No
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 Age60 YR
Patient SexMale
Patient Weight261 LB
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