Devices › Bed, ac-powered adjustable hospital
Device brand name · Ac-powered adjustable hospital bed
Resident Bed: medical device reports filed with FDA
292 reports name it, 2009–2017. Manufacturer given most often on reports: Hill-Rom. Product code FNL.
- 292
- device reports naming the brand
- 0% of all MAUDE reports · about 17 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 95.9%
- classified as malfunction
- 95.5% across the product code
- 2.4%
- classified as death, as reported
- 7 reports · not verified by FDA
FDA's MAUDE database holds 292 reports that name the brand "Resident Bed" (ac-powered adjustable hospital bed), received between January 2009 and October 2017; the manufacturer given most often on reports is Hill-Rom. Spellings of one product vary from report to report.
0 reports arrived in the 12 months to August 2026, and none in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (95.9%), death (2.4%) and other (1%); across all bed, ac-powered adjustable hospital reports (product code FNL) death is recorded in 0.7% and malfunction in 95.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are sticking (51.4%), device inoperable (12.7%) and device slipped (6.2%). The patient problems coded most often are physical entrapment, laceration(s) and death. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
No report naming Resident Bed was received in the five years to August 2026; the latest was received in October 2017.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 94,202 reports carrying product code FNL. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Sticking | 150 | 51.4% | 9.7% |
| Device inoperablethe device could not be used | 37 | 12.7% | 5.1% |
| Device slipped | 18 | 6.2% | 16.6% |
| Mechanical problema mechanical problem | 17 | 5.8% | 2.8% |
| Unintended head motion | 17 | 5.8% | 4% |
| Breakthe device broke | 15 | 5.1% | 9.4% |
| Device operates differently than expectedthe device behaved unexpectedly | 13 | 4.5% | 5.5% |
| Unintended system motionthe device moved when it should not have | 10 | 3.4% | 5.3% |
| Insufficient device problem information | 8 | 2.7% | 0.6% |
| Unintended movement | 3 | 1% | 2.9% |
| Collapse | 2 | 0.7% | 0.4% |
| Device alarm system | 2 | 0.7% | 8.2% |
| Device remains activated | 2 | 0.7% | 0% |
| Human-device interface problem | 2 | 0.7% | 0% |
| Improper or incorrect procedure or method | 2 | 0.7% | 0.2% |
| Material integrity problema problem with the device material | 2 | 0.7% | 0.3% |
| Scratched material | 2 | 0.7% | 0.8% |
| Bent | 1 | 0.3% | 1.5% |
| Component falling | 1 | 0.3% | 0.3% |
| Cut in material | 1 | 0.3% | 0.6% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Physical entrapment | 8 | 2.7% |
| Laceration(s) | 7 | 2.4% |
| Deaththe patient died; cause not stated by this term | 5 | 1.7% |
| Falla fall | 2 | 0.7% |
| Injurya physical injury | 2 | 0.7% |
| No patient involvement | 2 | 0.7% |
| Abrasion | 1 | 0.3% |
| Asphyxia | 1 | 0.3% |
| Bone fracture(s) | 1 | 0.3% |
| Bruise/contusion | 1 | 0.3% |
| Head injurya head injury | 1 | 0.3% |
| Hemorrhage/blood loss/bleeding | 1 | 0.3% |
| Suffocation | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Resident Bed | Product code FNL | All MAUDE reports |
|---|---|---|---|
| Reports | 292 | 94,202 | 26,136,888 |
| Share of that pool | — | 0.3% | 0% |
| Classified as death, per 1,000 reports | 24 | 7 | 9 |
| Classified as injury | 0.3% | 2% | 36.2% |
| Classified as malfunction | 95.9% | 95.5% | 62.3% |
| Filed by the manufacturer | 100% | 97.6% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code FNL
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Totalcare | 6,661 | 0 | 0% |
| Versacare Bed | 4,725 | 0 | 0.2% |
| TotalCare Bed | 4,138 | 274 | 0% |
| Versacare | 3,303 | 0 | 0.1% |
| Secure 3 Med/Surg Bed | 2,484 | 0 | 0.1% |
| Versacare Frame | 2,372 | 0 | 0.2% |
| In Touch Zu | 2,342 | 0 | 0.1% |
| Centra Bed | 2,214 | 0 | 0.1% |
| Advanta Bed | 2,187 | 5 | 0.3% |
| CareAssist Bed | 2,106 | 49 | 0% |
| Ac-Powered Adjustable Hospital Bed Including Rails | 2,167 | 0 | 1.3% |
| Century Bed | 1,386 | 0 | 0.4% |
| Secure 3 Med/Surg Bedobs 01/13 | 1,348 | 8 | 0.1% |
| 4 Motor Advance Bed | 1,339 | 0 | 0.4% |
| Centrella Bed | 1,334 | 798 | 0.2% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Resident Bed reports
How many FDA reports name Resident Bed?
292 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
malfunction (95.9%), death (2.4%) and other (1%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
sticking (51.4%), device inoperable (12.7%), device slipped (6.2%), mechanical problem (5.8%) and unintended head motion (5.8%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Resident Bed was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.