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Advanta™2 Bed P1190ARecalls & reported problems

Hill-Rom de México, S. de R.L. de C.V. · Hospital Bed · Class 2

Quick summary

This Hill-Rom Advanta 2 hospital bed has 85 reports in the FDA database, with no deaths and no injuries recorded. Many reports describe the bed moving or the head of the bed lowering on its own, and some describe torn material, CPR controls not working and alarms that did not sound. No recalls name this device.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
87
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 87 adverse event reports that list this exact device (DI 00887761000933), received between Oct 23, 2024 and Sep 28, 2026 — classified as 87 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (54 reports).

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 2 reportsNov 2024: 1 reportsDec 2024: 1 reportsJan 2025: 6 reportsFeb 2025: 2 reportsMar 2025: 6 reportsApr 2025: 8 reportsMay 2025: 6 reportsJun 2025: 1 reportsJul 2025: 3 reportsAug 2025: 7 reportsSep 2025: 3 reportsOct 2025: 5 reportsNov 2025: 5 reportsDec 2025: 1 reportsJan 2026: 5 reportsFeb 2026: 3 reportsMar 2026: 3 reportsApr 2026: 7 reportsMay 2026: 1 reportsJun 2026: 2 reportsJul 2026: 4 reportsAug 2026: 1 reportsSep 2026: 4 reportsOct 2026: 0 reports2024202520268
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Unintended Movement54
  • Material Split, Cut or Torn17
  • Activation Problem6
  • Collapse3
  • No Audible Alarm3
  • Material Frayed2
  • Activation Failure1
  • Defective Alarm1

Patient problems

  • No Clinical Signs, Symptoms or Conditions87

Recent adverse event reports

The 25 most recent of 87 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 28, 2026Unintended Movement

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50924540 ↗
  • MalfunctionSep 24, 2026Unintended Movement

    Baxter received a report that the ADVANTA2 RENTAL BED brake will not work while in brake position. This occurred during patient use. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50886554 ↗
  • MalfunctionSep 16, 2026Unintended Movement

    Baxter received a report that ADVANTA2 RENTAL BED had brakes not holding. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50791949 ↗
  • MalfunctionSep 3, 2026Activation Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50593087 ↗
  • MalfunctionAug 7, 2026Activation Failure

    Baxter received a report that the ADVANTA 2 FRAME had CPR functions not working. This occurred during Testing. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50182893 ↗
  • MalfunctionJul 21, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25899004 ↗
  • MalfunctionJul 21, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25893251 ↗
  • MalfunctionJul 15, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25833824 ↗
  • MalfunctionJul 6, 2026Unintended System Motion

    BAXTER RECEIVED A REPORT THAT ADVANTA2 RENTAL BED HAD HEAD OF THE BED WILL GO DOWN ON ITS OWN. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25728028 ↗
  • MalfunctionJun 11, 2026Activation Problem

    BAXTER RECEIVED A REPORT THAT ADVANTA FRAME HAD CPR FUNCTION NOT WORKING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25480595 ↗
  • MalfunctionJun 2, 2026Unintended Movement

    BAXTER RECEIVED A REPORT THAT ADVANTA 2 FRAME HAD BED HEAD SECTION RAISES ON IT'S OWN. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25368782 ↗
  • MalfunctionMay 26, 2026Unintended Movement

    BAXTER RECEIVED A REPORT THAT ADVANTA 2 FRAME HAD BRAKES NOT HOLDING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25294495 ↗
  • MalfunctionApr 30, 2026Unintended Movement

    BAXTER RECEIVED A REPORT THAT ADVANTA2 RENTAL BED HAD BRAKES NOT HOLDING WHILE BRAKE ENGAGED. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25052489 ↗
  • MalfunctionApr 20, 2026Unintended Movement

    BAXTER RECEIVED A REPORT THAT ADVANTA 2 FRAME HAD BRAKES NOT HOLDING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24928164 ↗
  • MalfunctionApr 17, 2026Collapse

    BAXTER RECEIVED A REPORT THAT ADVANTA 2 FRAME HAD A BED FRAME COLLAPSE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24913499 ↗
  • MalfunctionApr 15, 2026Material Split, Cut or Torn

    BAXTER RECEIVED A REPORT THAT ADVANTA 2 FRAME HAD THE AUXILIARY POWER CORD DAMAGED WITH COPPER WIRE EXPOSED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24889376 ↗
  • MalfunctionApr 8, 2026Unintended Movement

    A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT ADVANTA 2 FRAME HAD AN ISSUE, HEAD SECTION LOWERED WHEN PLUGGED IN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24821376 ↗
  • MalfunctionApr 8, 2026Material Split, Cut or Torn

    BAXTER RECEIVED A REPORT THAT ADVANTA2 RENTAL BED HAD BRAKES NOT HOLDING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24818431 ↗
  • MalfunctionApr 6, 2026Collapse

    BAXTER RECEIVED A REPORT THAT ADVANTA 2 FRAME HAD SIDERAIL DAMAGED AND DETACHED FROM THE UNIT FRAME. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24795117 ↗
  • MalfunctionMar 30, 2026Activation Problem

    BAXTER RECEIVED A REPORT THAT ADVANTA 2 FRAME HAD CPR WON'T ENGAGE AND ACTIVATE. THIS OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24736453 ↗
  • MalfunctionMar 30, 2026Unintended Movement

    BAXTER RECEIVED A REPORT THAT ADVANTA 2 FRAME HAD THE BED MOVING ON ITS OWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24736227 ↗
  • MalfunctionMar 18, 2026Detachment of Device or Device Component

    ON 20-FEB-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT ADVANTA 2 FRAME (PRODUCT CODE P1190A000091, SERIAL NUMBER (B)(6)), HAD AN ISSUE, ACCOUNT STATED SIDERAIL DETACHED. THIS OCCURRED AFTER PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24631879 ↗
  • MalfunctionFeb 25, 2026Unintended Movement

    ON 28-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT ADVANTA 2 FRAME (PRODUCT CODE P1190A000037, SERIAL NUMBER (B)(6)), HAD HEAD OF THE BED MOVING BY ITSELF. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24446025 ↗
  • MalfunctionFeb 11, 2026Unintended Movement

    ON 15-JAN-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT ADVANTA 2 FRAME (PRODUCT CODE P1190A000253, SERIAL NUMBER (B)(6)), HAD MULTIPLE ARTICULATIONS MOVING ON THEIR OWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24318308 ↗
  • MalfunctionFeb 3, 2026Unintended Movement

    ON 09-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT ADVANTA 2 FRAME (PRODUCT CODE P1190A000016, SERIAL NUMBER (B)(6)), HAD BED HEAD SECTION MOVING UP AND DOWN BY ITSELF. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24248218 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.