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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Penumbra, Inc. Velocity Delivery Microcatheter; DQY

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Penumbra, Inc. Velocity Delivery Microcatheter; DQY Back to Search Results
Catalog Number VEL160STR
Medical Device Problem Code Fracture (1260)
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
Velocity Delivery Microcatheter
Common Device Name
DQY
Manufacturer (Section D)
Penumbra, Inc.
one penumbra place
alameda CA 94502
Manufacturer (Section G)
Penumbra, Inc.
one penumbra place
alameda CA 94502
Manufacturer Contact
veronica menezes
one penumbra place
alameda, CA 94502
+1(510)748-3200
MDR Report Key50550835
Report Number3005168196-2026-00288
Device Sequence Number10376471
Product Code DQY
UDI-Device Identifier00814548012629
UDI-Public00814548012629
Combination Product (Y/N)N
Initial Reporter StateKS
Initial Reporter CountryUS
PMA/510(K) Number
K100826
Number of Events Summarized1
Summary Report (Y/N)N
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) 09/01/2026
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 Catalogue NumberVEL160STR
Device Lot NumberF00017858
Was Device Available for Evaluation? No
Date Returned to Manufacturer08/10/2026
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/03/2026
Initial Report FDA Received Date09/01/2026
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured07/25/2025
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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