INVACARE® IVC™ SERIES HOMECARE BED 5410IVCRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841447102199), received between Mar 4, 2025 and Mar 4, 2025 — classified as 1 injury.

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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DEALER REPORTED THAT A PATIENT AT A FACILITY HAD AN UNWITNESSED FALL FROM A 5410IVC BED. IT WAS REPORTED THAT THE PATIENT TRIED TO SIT UP & HE FELL HEADFIRST FROM THE BED. THE PATIENT WAS FOUND BY FACILITY STAFF WITH HIS LEFT ARM STUCK BEHIND HIM BETWEEN THE RAIL & MATTRESS, WHILE HIS BODY WAS ON THE FLOOR. THE PATIENT WAS SENT TO THE HOSPITAL VIA EMS WHERE HE RECEIVED X-RAYS, AND IT WAS FOUND THAT HE HAD A FRACTURE OF THE LEFT DISTAL HUMERUS. THE PATIENT HAD SURGERY WHERE HE RECEIVED PLACEMENT OF A PLATE AND SCREW DEVICE WITH MULTIPLE SCREWS TRANSFIXING THE SUPRACONDYLAR FRACTURE OF THE LEFT HUMERUS, AND SURGICAL SKIN STAPLES WERE PLACED ALONG THE POSTERIOR ASPECT OF THE LEFT ELBOW.

  Patient problems: Bone Fracture(s); Physical Entrapment

  MAUDE report 21515420 ↗