|
Model Number N/A |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
|
Patient Problems
Pain (1994); Scar Tissue (2060); Distress (2329); Unspecified Tissue Injury (4559)
|
Event Date 06/16/2021 |
Event Type
Injury
|
Manufacturer Narrative
|
(b)(4).D10: cat# 00877503601 lot# 2916775 bioloxa® delta, ceramic femoral head, s, a¸ 36/-3.5, taper 12/14 multiple mdr reports were filed for this event, please see associated report: 0001825034-2023-02291.The product will not be returned to zimmer biomet for investigation.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.
|
|
Event Description
|
It was reported that approximately 15 years post implantation of a left total hip arthroplasty, the patient was revised due to alleged elevated metal ions resulting in injury, additional scar tissue formation, pain, tissue destruction, metal wear, metal poisoning, loss of enjoyment of life, limitation of daily activities, emotional trauma, distress, and physical disabilities.No additional information available.
|
|
Manufacturer Narrative
|
(b)(4).This follow-up report is being submitted to relay additional information.The following sections were updated/corrected: updated: d4; h2; h4.Corrected: b3; b5; d6; h6.B3 event date: 2022.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
|
|
Event Description
|
It was reported that approximately two years following a hip procedure, the patient experienced adverse symptoms of inflammation and tissue damage.It is unknown if the patient is scheduled for or has undergone a revision surgery to date.No additional information available.
|
|
Event Description
|
No further information is available at the time of this report.
|
|
Manufacturer Narrative
|
(b)(4).This follow-up report is being submitted to relay additional information.No product was returned or pictures provided; visual and dimensional evaluations could not be performed.Unable to confirm complaint as no product was returned or medical records were provided.Review of the device history record(s) identified no deviations or anomalies during manufacturing.Medical records were not provided.A definitive root cause cannot be determined.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
|
|
Search Alerts/Recalls
|
|
|