MAUDE Adverse Event Report: ENCORE MEDICAL L.P SL-PLUS AND SLR-PLUS; HEAD, FEMORAL 32/+12

Model Number 400-32-120

Device Problem Appropriate Term/Code Not Available (3191)

Patient Problem Joint Dislocation (2374)

Event Date 08/09/2021

Event Type  Injury  

Manufacturer Narrative

Additional reporting on this event will be provided as a supplemental report to this document as soon as it becomes available.

Event Description

Revision surgery - the patient was dislocating, so the head and poly were removed and replaced with a +5mm offset 10 degree poly and 36mm +7 delta option head.

Manufacturer Narrative

Manufacturer narrative: the reason for this revision surgery was reported as dislocation.The previous surgery and the surgery detailed in this event occurred 14.1 years apart.The healthcare professional indicated there was no delay in surgery and another suitable device was available for use.The revision surgery was completed as intended.The devices were disposed of at hospital and not made available to djo surgical for examination.A review of the device history records (dhr) show that the reported components used in the previous surgery, when released for use, met design and manufacturing requirements.There were no non-conforming material reports (ncmr) associated with the products that may have contributed to the reported event.The devices were verified to have gone through an acceptable sterilization process and were within its expiration date at the time of the previous surgery.Customer complaint history of the reported devices showed no present trends or on-going issues that are needing a review.The root cause of this complaint was a revision surgery due to dislocation.There were no findings during this evaluation that indicate the reported devices were defective.No information was submitted with the complaint regarding pre-existing conditions of the patient or any activities the patient was involved in that may have contributed to the event.There are multiple factors that may contribute to an event that are outside the control of djo surgical.There are no indications of a product or process issue affecting implant safety or effectiveness.Additional reporting on this event will be provided as a supplemental report to this document if it becomes available.

• Brand Name: SL-PLUS AND SLR-PLUS
• Type of Device: HEAD, FEMORAL 32/+12
• Manufacturer (Section D): ENCORE MEDICAL L.P; 9800 metric blvd; austin TX 78758 5445
• MDR Report Key: 12365542
• MDR Text Key: 268078262
• Report Number: 1644408-2021-00885
• Device Sequence Number: 1
• Product Code: JDI
• UDI-Device Identifier: 00888912076395
• UDI-Public: (01)00888912076395
• Combination Product (y/n): N
• PMA/PMN Number: K932481
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Type of Report: Initial,Followup
• Report Date: 09/16/2021

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
• Device Operator: Health Professional
• Device Expiration Date: 12/28/2011
• Device Model Number: 400-32-120
• Device Catalogue Number: 400-32-120
• Device Lot Number: 284302
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 08/09/2021
• Initial Date FDA Received: 08/25/2021
• Supplement Dates Manufacturer Received: 09/08/2021
• Supplement Dates FDA Received: 09/16/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Treatment: 010-55-025 LOT 538053530; 010-55-025 LOT 53805553; 433-32-208 LOT 280872; UNK-SURG LOT UNKNOWN; 010-55-025 LOT 538053530; UNK-SURG LOT UNKNOWN
• Patient Outcome(s): Required Intervention
• Patient Age: 78 YR