INVACARE® G-SERIES BED G5510Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841447102694), received between Mar 25, 2026 and Jul 31, 2026 — classified as 1 death, 1 injury.

The most frequently reported specific device problem is “Use of Device Problem” (1 report).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• DeathJul 31, 2026Use of Device Problem

  The end user was in a G5510 Bed, taking a nap, and didn't realize he had rolled over on the bed remote causing it to go up as far as it would go. When he put his foot down to answer the phone, he fell out of the bed head first. He shattered his pelvis and broke his hip. He pressed his life alert button and he was taken to the closest hospital. Due to his injuries, he was put in a nursing home under hospice and passed away.

  Patient problems: Head Injury; Hip Fracture

  MAUDE report 50098101 ↗
• InjuryMar 25, 2026Appropriate Device Problem Term/Code Not Available

  THE END USER STATED HE HAS A G5510 BED THAT IS 84 INCHES LONG AND THE VA GAVE HIM AN 80 INCHES LONG MATTRESS. HE INDICATED HIS BED NEEDS TO BE FIXED TO BE MADE 80 INCHES LONG. HE REPORTED THAT HIS PILLOW FALLS IN THE GAP BETWEEN THE HEADBOARD AND THE MATTRESS. HE STATED THIS HAS HURT HIS NECK AND THERE WAS A FRACTURE TO HIS SPINE. HE ADVISED THAT HE WILL BE HAVING A SURGICAL PROCEDURE.

  Patient problems: Vertebral Fracture

  MAUDE report 24689516 ↗