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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DePuy Ireland - 9616671 ATTUNE; Knee Femoral

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DePuy Ireland - 9616671 ATTUNE; Knee Femoral Back to Search Results
Catalog Number 150440208
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code Unspecified Infection (1930)
Date of Event 07/22/2026
Type of Reportable Event Serious Injury
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Brand Name
ATTUNE
Common Device Name
Knee Femoral
Manufacturer (Section D)
DePuy Ireland - 9616671
loughbeg ringaskiddy co.
cork
EI 
Manufacturer (Section G)
JTE Warsaw Mfg Site
700 orthopaedic drive
warsaw IN 46582
Manufacturer Contact
elba bello
700 orthopaedic dr.
warsaw, IN 46581
+1(908)386-3534
MDR Report Key50260199
Report Number1818910-2026-13982
Device Sequence Number10635498
Product Code JWH
UDI-Device Identifier10603295042310
UDI-Public(01)10603295042310(17)290131(10)J2130J
Combination Product (Y/N)N
Initial Reporter StateMI
Initial Reporter CountryUS
PMA/510(K) Number
K241000
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2019
Reporter Type Manufacturer
Report Source Health Professional,Company Representative,Distributor
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 Number150440208
Device Lot NumberJ2130J
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Initial Date Received by Manufacturer 07/22/2026
Initial Report FDA Received Date08/14/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured02/13/2019
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 Age80 YR
Patient SexMale
Patient Weight228 LB
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