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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. Bivona Tight to Shaft Tracheostomy Tube; Tube tracheostomy and tube cuff

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ICU Medical Healthcare Manufacturing S.A. de C.V. Bivona Tight to Shaft Tracheostomy Tube; Tube tracheostomy and tube cuff Back to Search Results
Catalog Number 670160
Medical Device Problem Code Fluid/Blood Leak (1250)
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
Bivona Tight to Shaft Tracheostomy Tube
Common Device Name
Tube tracheostomy and tube cuff
Manufacturer (Section D)
ICU Medical Healthcare Manufacturing S.A. de C.V.
ave 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 Key50829305
Report Number9617604-2026-00850
Device Sequence Number8543332
Product Code JOH
UDI-Device Identifier15021312006032
UDI-Public(01)15021312006032(17)291218(10)6068547
Combination Product (Y/N)N
Initial Reporter StateNA
Initial Reporter CountryCA
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
Type of Report Initial
Report Date (Section B) 09/18/2026
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 Lay User/Patient
Device Catalogue Number670160
Device Lot Number6068547
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/26/2026
Initial Report FDA Received Date09/18/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured02/17/2025
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 SexUnknown
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