Sizewise 12060308-230VRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00845699003976), received between Jun 3, 2025 and Jun 10, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Connection 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 10, 2026Insufficient Device Problem Information

  A PATIENT ELEVATED A BED FRAME INDEPENDENTLY, ATTEMPTED TO EXIT, AND SUBSEQUENTLY FELL, RESULTING IN A FRACTURE OF THE TIBIA AND FIBULA.

  Patient problems: Limb Fracture

  MAUDE report 25456988 ↗
• MalfunctionJun 3, 2025Connection Problem; Connection Problem

  CUSTOMER STATES BED ALARM WORKED BUT DID NOT SIGNAL THE DESK WHEN PATIENT FELL OUT OF BED. NO PATIENT INJURIES WERE SUSTAINED.

  Patient problems: Fall

  MAUDE report 22134330 ↗