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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HOUSTON LEAD MODEL 304

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HOUSTON LEAD MODEL 304 Back to Search Results
Model Number 304-20
Medical Device Problem Code Fracture (1260)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 06/18/2026
Type of Reportable Event Malfunction
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Brand Name
LEAD MODEL 304
Common Device Name
LEAD
Manufacturer (Section D)
HOUSTON
100 cyberonics boulevard
houston TX 77058
Manufacturer (Section G)
HOUSTON
100 cyberonics boulevard
suite 600
houston TX 77058
Manufacturer Contact
cindy scott
100 cyberonics blvd
suite 600
houston, TX 77058
2816672681
MDR Report Key25798222
Report Number1644487-2026-10827
Device Sequence Number15700103
Product Code LYJ
UDI-Device Identifier05425025750139
UDI-Public05425025750139
Combination Product (Y/N)N
Initial Reporter StateMN
Initial Reporter CountryUS
PMA/510(K) Number
P970003
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2017
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional,Company Representative
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 07/13/2026
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 Expiration Date02/20/2021
Device Model Number304-20
Device Lot Number204029
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 06/18/2026
Initial Report FDA Received Date07/13/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured02/22/2017
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 Age51 YR
Patient SexFemale
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