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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STERIS CORPORATION HARMONYAIR; EQUIPMENT BOOM

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STERIS CORPORATION HARMONYAIR; EQUIPMENT BOOM Back to Search Results
Model Number HARMONYAIR CEILING BOOMS
Medical Device Problem Code Detachment of Device or Device Component (2907)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 06/12/2026
Type of Reportable Event Malfunction
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Brand Name
HARMONYAIR
Common Device Name
EQUIPMENT BOOM
Manufacturer (Section D)
STERIS CORPORATION
2720 gunter park drive east
montgomery AL 36109
Manufacturer (Section G)
STERIS CORPORATION
2720 gunter park drive east
montgomery AL 36109
Manufacturer Contact
daniel davy
5960 heisley road
mentor, OH 44060
4402597401
MDR Report Key25761046
Report Number1043572-2026-00063
Device Sequence Number21278925
Product Code FQO
UDI-Device Identifier00724995156718
UDI-Public(01)00724995156718(11)241217
Combination Product (Y/N)N
Initial Reporter StateCA
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source User Facility
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 07/09/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device Health Professional
Device Model NumberHARMONYAIR CEILING BOOMS
Device Catalogue NumberHMSLM
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 06/12/2026
Initial Report FDA Received Date07/09/2026
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured12/17/2024
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Reuse
Patient Sequence Number1
Patient SexUnknown
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