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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Zimmer Biomet, Inc. G7 VIT E NEUTRAL LNR 40MM G; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

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Zimmer Biomet, Inc. G7 VIT E NEUTRAL LNR 40MM G; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Back to Search Results
Catalog Number 30104007
Medical Device Problem Code Difficult to Insert (1316)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 09/09/2026
Type of Reportable Event Malfunction
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Brand Name
G7 VIT E NEUTRAL LNR 40MM G
Common Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
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 Key50934706
Report Number0001822565-2026-03289
Device Sequence Number21213829
Product Code LPH
UDI-Device Identifier00889024519978
Combination Product (Y/N)N
Initial Reporter StateVA
Initial Reporter CountryUS
PMA/510(K) Number
K190660
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) 09/29/2026
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 Number30104007
Device Lot Number67786526
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 09/09/2026
Initial Report FDA Received Date09/29/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured03/14/2026
Is the Device Labeled for Single Use? (Y/N) Yes
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
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