CHATTANOOGA 8250Recalls & reported problems
Djo, LLC · TRITON DTS ADVANCED ACCESSORY PACKAGE · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912454414), received between Jun 18, 2021 and Jun 18, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended System Motion” (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
Device problems
- Unintended System Motion1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 18, 2021Unintended System Motion; Unintended System Motion
IT WAS REPORTED BY THE CLINIC THAT WHEN PATIENTS ARE ON LUMBAR DECOMPRESSION, THE MAX POUNDS ALLEGEDLY RAMPS ABOVE THE CLINICIAN'S SETTING.
Patient problems: Insufficient Information
MAUDE report 12029111 ↗
Other EQUIPMENT, TRACTION, POWERED devices
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- Decompression of Choice E9011Pivotal Health Solutions, Inc. · Equipment, Traction, Powered1 report
- Modpod 12.1000Hollywog, LLC · Equipment, Traction, Powered1 report
- CHATTANOOGA 4759Djo, LLC · EQUIPMENT, TRACTION, POWERED1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.