INVACARE® IVC™ SERIES HOMECARE BED 5410LOWRecalls & reported problems
Invacare Corporation · IVC FULL ELECTRIC LOW BED · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 2
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00841447102168), received between Apr 17, 2024 and Feb 5, 2026 — classified as 2 deaths, 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Physical Entrapment2
- Hip Fracture1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
DeathFeb 5, 2026Use of Device Problem
A HOSPICE PROVIDER REPORTED THAT AN ASSISTED LIVING FACILITY CALLED THEIR TELECARE SERVICE ON (B)(6) 2025 FOR A CHANGE IN THE PATIENT'S LOC (LEVEL OF CONSCIOUSNESS). UPON NURSE ARRIVAL, THE FACILITY STATED THAT THE PATIENT WAS FOUND ON THE FLOOR WITH HIS HEAD WEDGED BETWEEN THE MATTRESS AND RAILING, AND HE HAD FOAM COMING OUT OF HIS MOUTH. THE PATIENT WAS PRONOUNCED DECEASED. THE MEDICAL EXAMINER DETERMINED THAT THE CAUSE OF DEATH WAS DEMENTIA; CONTRIBUTING FACTORS WERE ATHEROSCLEROSIS AND HYPERTENSION IN A MANNER OF NATURAL DEATH. THE HOSPICE PROVIDER ADVISED THAT THE BED AND RAILS INVOLVED ARE INVACARE PRODUTS. THE BED IS A MODEL 5410LOW. THE MODEL AND LOT CODE OF THE RAILS IS UNKNOWN. THE MATTRESS IS NOT AN INVACARE PRODUCT; IT IS FROM DRIVE MEDICAL.
Patient problems: Physical Entrapment
MAUDE report 24267983 ↗DeathJul 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PER FDA MEDWATCH FORM, AN 80 YEAR OLD MALE WEIGHING 196LBS WAS FOUND DECEASED AND LYING ON THE FLOOR, WITH HIS ARM CAUGHT IN THE BED RAIL. THE PATIENT'S HEAD WAS ON THE FLOOR WITH HIS LOWER BODY SUSPENDED IN THE AIR.
Patient problems: Physical Entrapment
MAUDE report 22667167 ↗InjuryApr 17, 2024Use of Device Problem; Use of Device Problem
A FACILITY ADMINISTRATOR ADVISED THAT FACILITY STAFF REPORT THE PATIENT WAS RESTLESS THROUGH THE NIGHT. THE PATIENT WAS IN A 5410LOW BED WITH BOTH LEGS THROUGH THE SIDE RAILS, THEN SHE PULLED HER LEGS BACK THROUGH THE RAILS. WHEN A HEALTH ASSISTANT WENT TO BATHE THE PATIENT, SHE NOTICED THE PATIENT'S LEFT LEG WAS DEFORMED ABOVE THE KNEE. THE PATIENT WAS LYING IN BED CALMLY. A DOCTOR WAS NOTIFIED, AND THE PATIENT WAS TRANSFERRED TO THE ER AND HOSPITALIZED WITH A CLOSED DISPLACED COMMINUTED FRACTURE OF SHAFT OF LEFT FEMUR. THE PATIENT HAD SURGERY.
Patient problems: Hip Fracture
MAUDE report 19123807 ↗
Other Bed, therapeutic, ac-powered, adjustable home-use devices
- sentida 5-le 19-1155WISSNER-BOSSERHOFF GmbH · Bed, Therapeutic, Ac-Powered, Adjustable Home-Use1 recall0 reports
- sentida 6-le 19-1156WISSNER-BOSSERHOFF GmbH · Bed, Therapeutic, Ac-Powered, Adjustable Home-Use1 recall0 reports
- sentida 1 19-0990WISSNER-BOSSERHOFF GmbH · Bed, Therapeutic, Ac-Powered, Adjustable Home-Use1 recall0 reports
- sentida 5 19-1119WISSNER-BOSSERHOFF GmbH · Bed, Therapeutic, Ac-Powered, Adjustable Home-Use1 recall0 reports
- sentida 04 19-1152WISSNER-BOSSERHOFF GmbH · Bed, Therapeutic, Ac-Powered, Adjustable Home-Use1 recall0 reports
- sentida 03 19-1062WISSNER-BOSSERHOFF GmbH · Bed, Therapeutic, Ac-Powered, Adjustable Home-Use1 recall0 reports
- INVACARE® G-SERIES BED G5510Invacare Corporation · Bed, therapeutic, ac-powered, adjustable home-use1 death2 reports
- INVACARE® IVC™ SERIES HOMECARE BED 5410IVCInvacare Corporation · Bed, therapeutic, ac-powered, adjustable home-use1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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