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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Medtronic Xomed Inc. XPS® BLADE; BUR, EAR, NOSE AND THROAT

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Medtronic Xomed Inc. XPS® BLADE; BUR, EAR, NOSE AND THROAT Back to Search Results
Model Number 1882940HR
Medical Device Problem Code Break (1069)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 07/07/2026
Type of Reportable Event Malfunction
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Brand Name
XPS® BLADE
Common Device Name
BUR, EAR, NOSE AND THROAT
Manufacturer (Section D)
Medtronic Xomed Inc.
6743 southpoint dr n
jacksonville FL 32216
Manufacturer (Section G)
Medtronic Xomed Inc.
6743 southpoint dr n
jacksonville FL 32216
Manufacturer Contact
justin ellis
6743 southpoint drive north
jacksonville, FL 32216
+1(763)526-5677
MDR Report Key50094553
Report Number1045254-2026-01061
Device Sequence Number10368581
Product Code EQJ
UDI-Device Identifier00885074079813
UDI-Public(01)00885074079813(17)300326(10)0233531941
Combination Product (Y/N)N
Initial Reporter CountryTW
PMA/510(K) Number
EXEMPT
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 07/30/2026
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 Model Number1882940HR
Device Catalogue Number1882940HR
Device Lot Number0233531941
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 07/07/2026
Initial Report FDA Received Date07/31/2026
Date Device Manufactured03/27/2026
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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