Voalte Nurse CallRecalls & reported problems across all models
Hill-Rom, Inc. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 419
- Deaths reported
- 2
- Injuries reported
- 10
- Recalls
- 2
We found 2 models of Voalte Nurse Call by Hill-Rom, Inc. in the FDA's device registry (GUDID). Together they are named in 419 adverse event reports in the FDA's MAUDE database, received between Aug 8, 2022 and Sep 29, 2026 — classified as 2 deaths, 10 injuries, 407 malfunctions.
The most frequently reported specific device problem is “Device Alarm System” (408 reports).
2 FDA recall records name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Voalte Nurse Call recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Apr 13, 2022Terminated
Firm discovered a firmware memory leak with a supplier-manufactured component.
Z-1094-2022 · Root cause: Software design · Recall details · FDA record ↗
- Oct 14, 2021Terminated
An unrecoverable error may occur where a component will fail to complete the reboot cycle, become non-functional and must be replaced.
Z-0402-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported Voalte Nurse Call problems
Device problems
- Device Alarm System408
- Defective Alarm4
- Alarm Not Visible2
- No Audible Alarm2
- Activation Problem1
- Audible Prompt/Feedback Problem1
- Failure to Sense1
- Material Split, Cut or Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions404
- Fall3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
- Bone Fracture(s)2
- Head Injury2
- Laceration(s)2
- Abrasion1
- Hematoma1
Voalte Nurse Call models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Voalte Nurse Call 4.0System, communication, powered2 recalls2 deaths405 reports
- Voalte Nurse Call 4.1System, communication, powered14 reports
Recent Voalte Nurse Call adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Device Alarm System
Baxter received a report stating the NURSE CALL INSTALLATION Bed exit alarm was not going to mobile devices or to the main console. The process step during which this occurred was unknown. There was no patient injury or death reported with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50927542 ↗MalfunctionSep 24, 2026Device Alarm System
Baxter received a report stating the NURSE CALL INSTALLATION code blue got the wrong location in the screen when they activated it. This occurred during patient use. There was no patient injury or death reported with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50888539 ↗MalfunctionSep 3, 2026Device Alarm System
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50598457 ↗MalfunctionAug 16, 2026Device Alarm System
Baxter received a report stating the NURSE CALL INSTALLATION bed exit alert is not showing in the dome light and the grs10. This occurred during patient use. There was no patient injury or death reported with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50266214 ↗MalfunctionAug 13, 2026Device Alarm System
Baxter received a report stating the NURSE CALL INSTALLATION code blue was not showing in pbx grs10. This occurred during patient use. There was no patient injury or death reported with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50231773 ↗MalfunctionAug 12, 2026Device Alarm System
Baxter received a report stating the NURSE CALL INSTALLATION bed exit alarm was not annunciating. The process step during which this occurred was unknown. There was no patient injury or death reported with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50230149 ↗MalfunctionAug 11, 2026Device Alarm System
Baxter received a report stating the NURSE CALL SERVER bed exit alert did not announce. This occurred during patient use. There was no patient injury or death reported with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50203834 ↗MalfunctionAug 7, 2026Device Alarm System
Baxter received a report stating the NURSE CALL INSTALLATION Bed exit alarms were not alerting to nurse station intermittently. The process step during which this occurred was unknown. There was no patient injury or death reported with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50183169 ↗MalfunctionJul 3, 2026Device Alarm System
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE NURSE CALL INSTALLATION CODE CALL DID NOT ALERT TO SECONDARY LOCATION. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT INJURY OR DEATH REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25709042 ↗MalfunctionJul 3, 2026Device Alarm System
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE NURSE CALL INSTALLATION BED EXIT CALL WAS ALERTING AS A REGULAR CALL. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT INJURY OR DEATH REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25707697 ↗MalfunctionJul 3, 2026Device Alarm System
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE NURSE CALL INSTALLATION GRS5 WOULD NOT RESPOND WHEN PULLED. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT INJURY OR DEATH REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25707102 ↗MalfunctionJul 2, 2026Device Alarm System
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE NURSE CALL INSTALLATION DURESS CALL DID NOT ANNUNCIATE.THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25691762 ↗MalfunctionJun 26, 2026Device Alarm System
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT NURSE CALL INSTALLATION BED EXIT ALERT WAS NOT TRIGGERING INSIDE THE ROOM. THERE WAS NO PATIENT INJURY OR DEATH REPORTED WITH THIS EVENT. IT WAS UNKNOWN IF ANY SECOND DEVICE WAS ALSO INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25632614 ↗MalfunctionJun 26, 2026Device Alarm System
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT NURSE CALL INSTALLATION CODE BLUE CALLS WERE NOT ALERTING AT HALLWAY.THERE WAS NO PATIENT INJURY OR DEATH REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25632573 ↗MalfunctionJun 23, 2026Device Alarm System
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE NURSE CALL INSTALLATION HAD THE CODE BLUE CALL NOT ANNUNCIATING. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25598223 ↗
Other Hill-Rom, Inc. products
- Centrella Bed2 models · 2,021 reports · 2 recalls
- VersaCare Med Surg Bed2 models · 1,200 reports
- pro+18 models · 36 reports · 13 recalls
- ALLEN24 models · 73 reports · 5 recalls
- WatchCare4 models · 0 reports · 4 recalls
- NaviCare Nurse Call Systems3 models · 99 reports · 2 recalls
- CompellaSurface3 models · 87 reports · 1 recall
- Progressa Surface13 models · 8 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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