Devices › Bed, ac-powered adjustable hospital
Device brand name · Bed ac-powered adjustable hospital
Versacare Frame: medical device reports filed with FDA
2,372 reports name it, 2013–2025. Manufacturer given most often on reports: Hill-Rom Batesville. Product code FNL.
- 2,372
- device reports naming the brand
- 0% of all MAUDE reports · about 177 a year
- 0
- reports, 12 months to August 2026
- 43 in the 12 months before
- 98.9%
- classified as malfunction
- 95.5% across the product code
- 0.2%
- classified as death, as reported
- 4 reports · not verified by FDA
FDA's MAUDE database holds 2,372 reports that name the brand "Versacare Frame" (bed ac-powered adjustable hospital), received between February 2013 and June 2025; the manufacturer given most often on reports is Hill-Rom Batesville. Spellings of one product vary from report to report.
0 reports arrived in the 12 months to August 2026, against 43 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 (98.9%), injury (0.9%) and death (0.2%); 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 device alarm system (30.4%), no audible alarm (20.9%) and material split, cut or torn (14.1%). The patient problems coded most often are no patient involvement, fall and hip fracture. 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
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
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 |
|---|---|---|---|
| Device alarm system | 720 | 30.4% | 8.2% |
| No audible alarm | 495 | 20.9% | 1.9% |
| Material split, cut or torn | 335 | 14.1% | 4.3% |
| Defective alarm | 279 | 11.8% | 0.6% |
| Unintended movement | 220 | 9.3% | 2.9% |
| Device slipped | 80 | 3.4% | 16.6% |
| Self-activation or keying | 40 | 1.7% | 0.5% |
| Unintended system motionthe device moved when it should not have | 38 | 1.6% | 5.3% |
| Device operates differently than expectedthe device behaved unexpectedly | 32 | 1.3% | 5.5% |
| Device displays incorrect message | 23 | 1% | 0.6% |
| Unintended head motion | 21 | 0.9% | 4% |
| Activation problem | 16 | 0.7% | 0.3% |
| Material frayed | 16 | 0.7% | 0.4% |
| Device inoperablethe device could not be used | 12 | 0.5% | 5.1% |
| Defective component | 10 | 0.4% | 0.2% |
| Communication or transmission problemthe device could not communicate or transmit | 9 | 0.4% | 0.2% |
| Loose or intermittent connection | 9 | 0.4% | 0.4% |
| Breakthe device broke | 8 | 0.3% | 9.4% |
| Intermittent continuity | 7 | 0.3% | 0% |
| Mechanical problema mechanical problem | 7 | 0.3% | 2.8% |
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 |
|---|---|---|
| No patient involvement | 638 | 26.9% |
| Falla fall | 8 | 0.3% |
| Hip fracturea broken hip | 5 | 0.2% |
| Bone fracture(s) | 4 | 0.2% |
| Pressure sore/ulcer | 4 | 0.2% |
| Bone cement implantation syndrome | 1 | 0% |
| Deaththe patient died; cause not stated by this term | 1 | 0% |
| Disc impingement | 1 | 0% |
| Electric shockan electric shock | 1 | 0% |
| Hemorrhage, subarachnoid | 1 | 0% |
| Hemorrhage, subdural | 1 | 0% |
| Laceration(s) | 1 | 0% |
| Stroke/cva | 1 | 0% |
| Wound infectionan infected wound | 1 | 0% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Versacare Frame | Product code FNL | All MAUDE reports |
|---|---|---|---|
| Reports | 2,372 | 94,202 | 26,136,888 |
| Share of that pool | — | 2.5% | 0% |
| Classified as death, per 1,000 reports | 2 | 7 | 9 |
| Classified as injury | 0.9% | 2% | 36.2% |
| Classified as malfunction | 98.9% | 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% |
| 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% |
| Progressa Frame | 1,207 | 7 | 0.1% |
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 Versacare Frame reports
How many FDA reports name Versacare Frame?
2,372 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 (98.9%), injury (0.9%) and death (0.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device alarm system (30.4%), no audible alarm (20.9%), material split, cut or torn (14.1%), defective alarm (11.8%) and unintended movement (9.3%). 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 Versacare Frame 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.