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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Zimmer Biomet, Inc. PERSONA FEM CR IMPACTOR PAD; Instrument, Knee

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Zimmer Biomet, Inc. PERSONA FEM CR IMPACTOR PAD; Instrument, Knee Back to Search Results
Catalog Number 42509909400
Medical Device Problem Code Fracture (1260)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 07/22/2026
Type of Reportable Event Malfunction
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Brand Name
PERSONA FEM CR IMPACTOR PAD
Common Device Name
Instrument, Knee
Manufacturer (Section D)
Zimmer Biomet, Inc.
1800 w. center st.
warsaw IN 46580
Manufacturer (Section G)
Zimmer Biomet, Inc.
1800 w. center st.
warsaw IN 46580
Manufacturer Contact
jennifer rapsavage
56 e. bell dr.
warsaw, IN 46582
+1(574)526-0384
MDR Report Key50226240
Report Number0001822565-2026-02839
Device Sequence Number10292515
Product Code MBH
UDI-Device Identifier00889024232891
UDI-Public(01)00889024232891(10)66152770
Combination Product (Y/N)N
Initial Reporter StateGA
Initial Reporter CountryUS
PMA/510(K) Number
K172524
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional,Distributor
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 08/10/2026
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 Number42509909400
Device Lot Number66152770
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 07/24/2026
Initial Report FDA Received Date08/12/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured10/05/2023
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
Patient Sequence Number1
Patient SexMale
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