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EasyStand StrapStandRecalls & reported problems

Altimate Medical Inc. · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10858921006086), received between Apr 25, 2019 and Apr 25, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Inadequate or Insufficient Training” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Inadequate or Insufficient Training1

Patient problems

  • Bone Fracture(s)1
  • Hematoma1

Recent adverse event reports

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

  • InjuryApr 25, 2019Inadequate or Insufficient Training; Inadequate or Insufficient Training

    RECEIVED A PHONE CALL FROM A FACILITY STATING THAT A CLIENT HAD FALLEN BACK IN A STRAPSTAND. THE PRODUCT SERIAL NUMBER WAS PROVIDED AND THE UNIT REVIEWED. THE PRODUCT THAT WAS ORDERED BY THE FACILITY WAS A BASIC STRAPSTAND. VARIOUS QUESTIONS WERE ASKED TO OBTAIN MORE INFORMATION, AND THE FOLLOWING INFORMATION WAS OBTAINED: THE CLIENT FELL BACK "LIKE YOU WOULD FALL BACK IN A SWING" WITH BUTTOCKS IN THE SLING AND BACK OF HEAD HITTING THE FLOOR. WHEN STANDING THE STRAP SLID DOWN . WHEN ASKED IF THE WHEELCHAIR WAS POSITIONED UNDERNEATH THE CLIENT, SHE SAID NO, BECAUSE WHEN THE WHEELCHAIR WAS WHEELED UP TO THE STANDER IT DID NOT FIT IN BETWEEN THE LEGS OF THE UNIT. I INFORMED HER THAT DUE TO DIFFERENT WHEELCHAIR WIDTHS, THERE ARE STANDARD LEGS AND SWING AWAY LEGS AND THAT THE STANDARD LEGS WERE WHAT WAS ORDERED. SHE SAID WHEN THE WHEELCHAIR DIDN'T GO IN BETWEEN THE LEGS OF THE UNIT THAT 3 OF THEM TRIED TO PUT THE CLIENT IN THE STANDER, BY HAVING ONE PERSON ON EACH SIDE OF HIM AND ONE PERSON PUTTING ON THE STRAP. THE CONTACT WAS ASKED IF THEY SAW AN INSERVICE OF THE PRODUCT OR IF THE UNIT WAS SPEC'D OUT BEFORE ORDERING AND SHE SAID NO THEY JUST ORDERED IT OUT OF A CATALOG. THE CONTACT WA

    Patient problems: Bone Fracture(s); Hematoma

    MAUDE report 8551437 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.