MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US ACTIS COLLARED HIGH SIZE 9; HIP FEMORAL STEM

Model Number 1010-12-090

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Fall (1848); Bone Fracture(s) (1870)

Event Date 12/11/2020

Event Type  Injury  

Manufacturer Narrative

Product complaint #: (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

It was reported that the patient suffered a fall causing a proximal femur fracture.Surgeon removed the actis size 9 hi offset stem, 36+8.5 metal ball, and 36x58 neutsl liner.A reclaim stem was placed with a 36+5 ball and a 36x58 lipped liner.No surgical delay.Doi: (b)(6) 2020, dor: (b)(6) 2020, 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.Device history lot : the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.

• Brand Name: ACTIS COLLARED HIGH SIZE 9
• Type of Device: HIP FEMORAL STEM
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 11087047
• MDR Text Key: 224053511
• Report Number: 1818910-2020-27708
• Device Sequence Number: 1
• Product Code: KWL
• UDI-Device Identifier: 10603295380610
• UDI-Public: 10603295380610
• Combination Product (y/n): N
• PMA/PMN Number: K150862
• 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: 12/11/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/29/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: No Information
• Device Model Number: 1010-12-090
• Device Catalogue Number: 101012090
• Device Lot Number: J71U51
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 01/26/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Treatment: ALTRX NEUT 36IDX58OD; ARTICULEZE M HEAD 36MM +8.5; ALTRX NEUT 36IDX58OD; ARTICULEZE M HEAD 36MM +8.5
• Patient Outcome(s): Required Intervention
• Patient Age: 89 YR