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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DePuy Orthopaedics Inc US ATTUNE; Knee Stems

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DePuy Orthopaedics Inc US ATTUNE; Knee Stems Back to Search Results
Catalog Number 151314060
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code Pain (1994)
Date of Event 09/17/2026
Type of Reportable Event Serious Injury
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Brand Name
ATTUNE
Common Device Name
Knee Stems
Manufacturer (Section D)
DePuy Orthopaedics Inc US
700 orthopaedic drive
warsaw IN 46581 -098
Manufacturer (Section G)
JTE Warsaw Mfg Site
700 orthopaedic drive
warsaw IN 46582
Manufacturer Contact
elba bello
700 orthpaedic dr.
warsaw, IN 46581
+1(908)386-3534
MDR Report Key50904677
Report Number1818910-2026-16641
Device Sequence Number6026749
Product Code JWH
UDI-Device Identifier10603295043607
UDI-Public(01)10603295043607(17)340831(10)D24083038
Combination Product (Y/N)N
Initial Reporter StateID
Initial Reporter CountryUS
PMA/510(K) Number
K241000
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2025
Device Explanted Year2026
Reporter Type Manufacturer
Report Source Health Professional,Company Representative
Initial Reporter Occupation Physician
Type of Report Initial
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device Health Professional
Device Catalogue Number151314060
Device Lot NumberD24083038
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Initial Date Received by Manufacturer 09/18/2026
Initial Report FDA Received Date09/25/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured09/01/2024
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
Outcome Attributed to Adverse Event Required Intervention;
Patient SexFemale
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