Sonesta 6210Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07350006950018), received between Jan 9, 2026 and Jan 9, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Missing Information” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Aug 22, 2025Open, Classified

   Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.

   Z-0460-2026 · Root cause: Process control · FDA record ↗

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.

• InjuryJan 9, 2026Missing Information

  DURING POST-PROCEDURE PATIENT CARE, A PARAPLEGIC PATIENT WAS REPOSITIONED WHILE SEATED ON A MODEL 6210 PROCEDURE CHAIR. DURING DRESSING, THE PATIENT WAS LEANED AGAINST A DETACHABLE ARM REST. THE ARM REST IS INTENDED FOR PATIENT COMFORT AND ARM POSITIONING AND IS NOT DESIGNED TO SUPPORT PATIENT BODY WEIGHT. DURING THIS MANEUVER, THE ARM REST ATTACHMENT CAME LOOSE, AND THE PATIENT FELL FROM THE CHAIR TO THE FLOOR. TWO HEALTHCARE STAFF MEMBERS SUSTAINED BACK INJURIES WHILE ATTEMPTING TO PREVENT THE FALL. ONE STAFF INJURY REQUIRED MEDICAL CARE AND RESULTED IN WORK RESTRICTIONS. THE PATIENT WAS EVALUATED FOLLOWING THE FALL AND NO ACUTE INJURY WAS REPORTED.

  Patient problems: Back pain

  MAUDE report 24018512 ↗