Decompression of Choice E9011Recalls & reported problems
Pivotal Health Solutions, Inc. · Swing arm DOC table, 115V · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00852753008907), received between Oct 15, 2025 and Oct 15, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Mechanical Problem” (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.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 15, 2025Mechanical Problem; Mechanical Problem
A WELD ON PART E7130 APPEARS TO HAVE FAILED AND THE PIECE OF THE TABLE CONNECTED THROUGH THE E7130 WELD FELL TO THE GROUND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23291041 ↗
Other Equipment, Traction, Powered devices
- CHATTANOOGA 2841Djo, LLC · EQUIPMENT, TRACTION, POWERED5 reports
- CHATTANOOGA 8250Djo, LLC · EQUIPMENT, TRACTION, POWERED1 report
- Modpod 12.1000Hollywog, LLC · Equipment, Traction, Powered1 report
- CHATTANOOGA 4759Djo, LLC · EQUIPMENT, TRACTION, POWERED1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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