MAUDE Adverse Event Report: ENCORE MEDICAL L.P. ACETABULAR HIP; TRIAL LINER, EMPOWR ACETABULAR, 10°, 40G

Model Number	803-42-40G
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	07/20/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional reporting on this event will be provided as a supplemental report to this document as soon as it becomes available.
Event or Problem Description
Instrument failure, liner was damaged and not locking appropriately.It needs replacement.

• Brand Name: ACETABULAR HIP
• Common Device Name: TRIAL LINER, EMPOWR ACETABULAR, 10°, 40G
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd; austin, tx 78758-5445
• MDR Report Key: 12483018
• Report Number: 1644408-2021-00978
• Device Sequence Number: 17433178
• Product Code: LPH
• UDI-Device Identifier: 00190446296584
• UDI-Public: (01)00190446296584
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K190057
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 09/16/2021

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 Model Number: 803-42-40G
• Device Catalogue Number: 803-42-40G
• Device Lot Number: 283658L17
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/20/2021
• Initial Report FDA Received Date: 09/16/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other