Persona® 42-5706-066-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024576513), received between Dec 13, 2022 and Dec 13, 2022 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 13, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT UNDERWENT AN INITIAL LEFT TOTAL KNEE ARTHROPLASTY. APPROXIMATELY 7 DAYS POST IMPLANTATION, THE PATIENT PRESENTED WITH SHORTNESS OF BREATH. THE PATIENT WAS ADMITTED FOR PULMONARY EMBOLISM WITHOUT ACUTE COR PULMONALE, ELEVATED TROPONINS, AND ACUTE MYOCARDIAL INJURY. THE PATIENT WAS PLACED ON ADDITIONAL ANTICOAGULANTS AND OXYGEN AND DISCHARGED 3 DAYS LATER. APPROXIMATELY 2 WEEKS LATER, THE PATIENT WAS DIAGNOSED WITH DEEP VEIN THROMBOSIS OF THE LEFT CALF. THE PATIENT IS TAKING ELIQUIS. NO FURTHER COMPLICATIONS WERE REPORTED AT THIS TIME.

  Patient problems: Cardiac Enzyme Elevation; Hypoxia; Pulmonary Embolism; Thrombosis/Thrombus

  MAUDE report 15971301 ↗