EasyStand Bantam MediumRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10858921006055), received between Jun 26, 2020 and Jun 26, 2020 — classified as 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 16, 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.

• InjuryJun 26, 2020Use of Device Problem; Use of Device Problem

  ON (B)(6) 2020 QUALITY PERSONNEL RECEIVED AN EMAIL ABOUT AN INJURY TO AN EMPLOYEE OF A MEDICAL EQUIPMENT DEALER. ON (B)(6) 2020 A PHONE CALL WAS MADE TO GATHER MORE INFORMATION ABOUT THE INJURY. THE INJURY TO THE EMPLOYEE OCCURRED WHEN THE INDIVIDUAL WORKING WITH THE UNIT WAS LOWERING THE EMPTY UNIT FROM THE STANDING POSITION. IN THIS CASE THE INDIVIDUAL GRABBED THE HIP BRACKET AND ABOUT A QUARTER OF THE WAY DOWN THE INDIVIDUAL'S THUMB WAS PINCHED BETWEEN THE HIP BRACKET AND THE HIP GUIDE KNOB. THE INDIVIDUAL RECEIVED A CUT TO THEIR THUMB WHICH NEEDED STITCHES TO REPAIR.

  Patient problems: Laceration(s)

  MAUDE report 10200463 ↗