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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US PINN MAR +4 10D 32IDX54OD; PINNACLE HIP SYSTEM : HIP POLY ACETABULAR LINERS

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DEPUY ORTHOPAEDICS INC US PINN MAR +4 10D 32IDX54OD; PINNACLE HIP SYSTEM : HIP POLY ACETABULAR LINERS Back to Search Results
Model Number 1219-32-154
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes Pain (1994); No Code Available (3191)
Date of Event 10/05/2020
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
 
Event or Problem Description
Revision of corail stem to corail revision on (b)(6) 2020.Change of liner, change head.Revision due to pain and joint instability secondary to loosening of the femoral stem.No reported surgical delay or patient complications.
 
Additional Manufacturer Narrative
Product complaint # : (b)(4).Investigation summary : no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed, and the investigation will be re-opened as necessary.Device history lot : per (b)(4), a mre is unlikely to add value to the complaint investigation regarding an allegation of pain.
 
Additional Manufacturer Narrative
Product complaint # (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes joint reconstruction, or its employees that the report constitutes an admission that the product, depuy synthes joint reconstruction, or its employees caused or contributed to the potential event described in this report.H10 additional narrative: added: b5, d4 (lot), h4.Corrected: a2 (age).If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.
 
Event or Problem Description
Additional information received indicated that the affected side is the right side.
 
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Brand Name
PINN MAR +4 10D 32IDX54OD
Common Device Name
PINNACLE HIP SYSTEM : HIP POLY ACETABULAR LINERS
Manufacturer (Section D)
DEPUY ORTHOPAEDICS INC US
700 orthopaedic drive
warsaw IN 46581 0988
MDR Report Key10698458
Report Number1818910-2020-22772
Device Sequence Number3899498
Product Code LPH
UDI-Device Identifier10603295014065
UDI-Public10603295014065
Combination Product (Y/N)N
Initial Reporter CountryAS
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2012
Device Explanted Year2020
Serviced by Third Party (Y/N)Unknown
Reporter Type Manufacturer
Report Source company representative,foreig
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup,Followup
Report Date (Section B) 10/05/2020
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 Model Number1219-32-154
Device Catalogue Number121932154
Device Lot Number200654
Was Device Available for Evaluation? No
Initial Date Received by Manufacturer 10/05/2020
Supplement Date Received by Manufacturer10/20/2020
12/10/2020
Initial Report FDA Received Date10/19/2020
Supplement Report FDA Received Date11/03/2020
12/15/2020
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Concomitant Medical Products
and Therapy/Usage Dates
ARTICUL/EZE BALL 32 +5 BR; CORAIL AMT SZ9 135 HIGH COL; PINN MAR +4 10D 32IDX54OD; ARTICUL/EZE BALL 32 +5 BR; CORAIL AMT SZ9 135 HIGH COL; PINN MAR +4 10D 32IDX54OD
Outcome Attributed to Adverse Event Required Intervention;
Patient Age67 YR
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