Trident 2850HD-22Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383531069), received between Mar 15, 2019 and Mar 15, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Device Damaged Prior to Use” (1 report).

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.

• InjuryMar 15, 2019Device Damaged Prior to Use; Device Damaged Prior to Use

  (B)(6) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A POWER CHAIR. THE END-USER HAD THE SEAT FOR APPROXIMATELY A YEAR, HE NOTICED A TEAR IN THE SEAT IN DECEMBER BUT CONTINUED TO USE THE DEVICE. PROVIDER CALLED STATING AN END USER SUFFERED AN INJURY USING THE TRIDENT HD. END USER WAS RECLINING THE CHAIR WHEN ALL OF A SUDDEN HE WAS CUT IN THE BACK BY WHAT THEY BELIEVE IS THE SEAT RECLINING MECHANISM. IT PUNCTURED THROUGH THE BACK SEAT SOMEHOW, AND CUT (B)(6) LEAVING ABOUT A 2" GASH. HE WENT TO THE HOSPITAL TO GET TREATED AND RECEIVED STITCHES. (B)(6) WENT TO THE HOSPITAL AND RECEIVED 3 BUTTERFLY STITCHES WHILE HE IS CURRENTLY ON BLOOD THINNERS.

  Patient problems: Laceration(s)

  MAUDE report 8426005 ↗