P500 Surface P005787RENT01SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887761999459), received between Jul 14, 2025 and Jan 30, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (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

Recent adverse event reports

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

• MalfunctionJan 30, 2026No Audible Alarm

  ON 05-JAN-2026, AN OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT P500 THERAPY SURFACE (PRODUCT CODE: P005787RENT01S, SERIAL NUMBER: (B)(6), HAD BED EXIT ALARM NOT WORKING, PATIENT FELL GETTING OUT OF BED. THIS OCCURRED DURING PATIENT USE. IT WAS REPORTED THAT NO INJURY OCCURRED FROM THE REPORTED EVENT.

  Patient problems: Fall

  MAUDE report 24225710 ↗
• MalfunctionJul 14, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE P500 THERAPY SURFACE POWER CORD WAS DAMAGED WITH COPPER WIRES EXPOSED. THE BED WAS LOCATED AT THE ACCOUNT. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22496465 ↗