T.E.D. 7115Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10192253015973), received between Oct 3, 2023 and Oct 3, 2023 — 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. How this data works · Data updated Oct 13, 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.

• InjuryOct 3, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THAT PERONEAL NERVE PALSY OCCURRED DURING USE OF TED SURGICAL STOCKINGS. TED WAS PUT ON THE PATIENT FOR TOTAL KNEE ARTHROPLASTY. LATER, THE PATIENT COMPLAINED OF NUMBNESS, AND THE PHYSICIAN WHO SAW THE PATIENT DIAGNOSED THEM AS HAVING PERONEAL NERVE PALSY. ADDITIONAL INFORMATION RECEIVED ON 02OCT2023 STATED THAT THE PATIENT HAS DROP FOOT AND POOR DORSIFLEXION DUE TO THIS INCIDENT. THE PATIENT IS CURRENTLY TAKING PHYSICAL THERAPY. THE NUMBNESS HAS DECREASED NOW. IT IS UNKNOWN HOW LONG THE NUMBNESS STAYED. NO OTHER SYMPTOMS WERE EXPERIENCED.

  Patient problems: Nerve Damage

  MAUDE report 17865213 ↗