Sizewise BRP3 394880Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00845699002238), received between Jun 5, 2025 and Sep 4, 2026 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

• InjurySep 4, 2026Unintended Movement

  The bed frame was stuck in an elevator and not working. Then the device went into reverse and kept backing into a Medical Center employee injuring their left shoulder and left upper back.

  Patient problems: Insufficient Information

  MAUDE report 50613467 ↗
• InjuryJun 5, 2025No Apparent Adverse Event; Insufficient Device Problem Information; No Apparent Adverse Event; Insufficient Device Problem Information

  HOSPITAL REPORTED STAFF MEMBER HAD SEVERE SHOULDER INJURY FROM ATTEMPTING TO MOVE THE BED AND RECEIVED TREATMENT AT ER. HOSPITAL REPORTED BED IN WORKING CONDITION AND PROCEEDED TO PLACE INTO PATIENT USE.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 22154438 ↗