Centrella SurfaceRecalls & reported problems across all models
Hill-Rom, Inc. · 5 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Centrella Surface model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 5 models of Centrella Surface by Hill-Rom, Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Jan 29, 2025 and Jan 29, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (1 report).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
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
Centrella Surface 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.
- May 8, 2024Open, Classified
There is a potential for the top cover of the hospital bed mattress to delaminate as a result of improper cleaning and lack of adequate details on the appropriate use of cleaning agents containing bleach.
Z-2151-2024 · Root cause: Error in labeling · names 4 of these models · Recall details · FDA record ↗
Most reported Centrella Surface problems
Device problems
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Centrella Surface models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Centrella™ Surface P7922ARENT01BED, FLOTATION THERAPY, POWERED1 recall0 reports
- Centrella™ Surface P7922A03BED, FLOTATION THERAPY, POWERED1 recall0 reports
- Centrella™ Surface P7922A02BED, FLOTATION THERAPY, POWERED1 recall0 reports
- Centrella™ Surface P7922A01BED, FLOTATION THERAPY, POWERED1 recall0 reports
- Centrella™ Surface P7922ARENT02BED, FLOTATION THERAPY, POWERED1 report
Recent Centrella Surface adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJan 29, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE CENTRELLA MAX MATTRESS, WIDE SIDERAIL FALSE LATCHES; WHEN APPLYING WEIGHT TO THE SIDERAIL MAKES IT COME DOWN. 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 21265773 ↗
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
- Voalte Nurse Call2 models · 419 reports · 2 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
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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