MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US DELTA CER HEAD 12/14 32MM +1; ARTICULEZE HEAD (12/14 TAPER) : HIP CERAMIC FEMORAL HEADS

Model Number 1365-32-310

Device Problem Device Dislodged or Dislocated (2923)

Patient Problems Joint Dislocation (2374); No Code Available (3191); Cancer (3262)

Event Date 05/12/2020

Event Type  Injury  

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 Description

The patient was revised to address progressive cancer and chronic dislocations leading to surgeon deciding to remove all implants.Doi: (b)(6) 2020; dor: (b)(6) 2020; affected side: right hip.

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.H10 additional narrative: added: b7 corrected: h6 (patient) removed code for cancer.H6 patient code: no code available (3191) was used to capture device revision or replacement.

• Brand Name: DELTA CER HEAD 12/14 32MM +1
• Type of Device: ARTICULEZE HEAD (12/14 TAPER) : HIP CERAMIC FEMORAL HEADS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 10093988
• MDR Text Key: 192368734
• Report Number: 1818910-2020-12689
• Device Sequence Number: 1
• Product Code: LZO
• UDI-Device Identifier: 10603295033431
• UDI-Public: 10603295033431
• Combination Product (y/n): N
• PMA/PMN Number: K031803
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,health
• Type of Report: Initial,Followup
• Report Date: 05/12/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 05/27/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 1365-32-310
• Device Catalogue Number: 136532310
• Device Lot Number: 9356109
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 07/09/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Treatment: ALTRX NEUT 32IDX48OD; CORAIL AMT COLLAR SIZE 13; DELTA CER HEAD 12/14 32MM +1; PROTRUSIO CAGE 48ODX45ID R; SLF TAPPING ROOF PILE SCRW20MM; SLF TAPPING ROOF PILE SCRW20MM; SLF TAPPING ROOF PILE SCRW25MM; SLF TAPPING ROOF PILE SCRW25MM; SLF TAPPING ROOF PILE SCRW30MM; SLF TAPPING ROOF PILE SCRW30MM; SLF TAPPING ROOF PILE SCRW30MM; SLF TAPPING ROOF PILE SCRW30MM; SLF TAPPING ROOF PILE SCRW35MM; SLF TAPPING ROOF PILE SCRW35MM
• Patient Outcome(s): Required Intervention
• Patient Age: 79 YR