MAUDE Adverse Event Report: ENCORE MEDICAL L.P ALTIVATE ANATOMIC SHOULDER; ALTIVATE ANATOMIC, SHORT HUMERAL STEM, 14MM

Model Number 520-14-000

Device Problems Patient-Device Incompatibility (2682); Appropriate Term/Code Not Available (3191)

Patient Problem Pain (1994)

Event Date 10/15/2020

Event Type  Injury  

Manufacturer Narrative

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

Event Description

Revision surgery - patient presented shoulder pain.Removed and exchanged all implants except for the glenoid.

Manufacturer Narrative

Manufacturer narrative: the reason for this revision surgery was reported as pain.The previous surgery and the surgery detailed in this event occurred 1 year 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 the hospital and not made available to djo surgical for examination.A review of the device history records (dhr) shows that the reported components used in the previous surgery, when released for use, met design and manufacturing requirements and showed no non-conforming material reports (ncmr) associated with the main contributor component listed in the complaint.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 pain.There were no other 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 such as poor bone density, patient bone deterioration, inadequate soft tissue support, patient activities or trauma.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: ALTIVATE ANATOMIC SHOULDER
• Type of Device: ALTIVATE ANATOMIC, SHORT HUMERAL STEM, 14MM
• Manufacturer (Section D): ENCORE MEDICAL L.P; 9800 metric blvd; austin,tx 78758-5445
• MDR Report Key: 10836328
• MDR Text Key: 216176756
• Report Number: 1644408-2020-01042
• Device Sequence Number: 1
• Product Code: KWS
• UDI-Device Identifier: 00190446176039
• UDI-Public: (01)00190446176039
• Combination Product (y/n): N
• PMA/PMN Number: K162024
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Type of Report: Initial,Followup
• Report Date: 12/21/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/13/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: 520-14-000
• Device Catalogue Number: 520-14-000
• Device Lot Number: 853U1162
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 11/23/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Treatment: 520-07-000 LOT 888U1347; 520-46-316 LOT 957U1089; 520-07-000 LOT 888U1347; 520-46-316 LOT 957U1089
• Patient Outcome(s): Required Intervention
• Patient Age: 58 YR