Rollstand 9770116Recalls & reported problems
Bard Access Systems, Inc. · BAS MEDICAL EQUIPMENT ROLL STAND (MER) · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00801741124693), received between Jul 17, 2018 and May 26, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem3
- Erratic or Intermittent Display1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 26, 2026Mechanical Problem
IT WAS REPORTED THAT THE WHEELS ON THE MER STAND ARE PULLING IN 1 DIRECTION AND THE USER CANNOT MOVE IT IN A STRAIGHT LINE. NO FURTHER DETAILS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25295149 ↗MalfunctionDec 16, 2021Mechanical Problem; Mechanical Problem
MER STAND HAS A BENT CASTER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13018103 ↗MalfunctionAug 4, 2021Mechanical Problem; Mechanical Problem
PER BIOMED, ONE OF THE CASTER WHEELS WILL NOT SIT STRAIGHT AND APPEARS TO BE BENT. THE STAND ROCKS AS THE WHEELS AREN'T LEVEL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12277306 ↗MalfunctionJul 17, 2018Erratic or Intermittent Display
IT WAS REPORTED BY THE BD TM THAT THE SR 8 WAS ON AN MER STAND AND BEING MANEUVERED OUT OF AN ELEVATOR WHEN THE WHEELS CAUGHT ON THE ELEVATOR THRESHOLD AND TIPPED OVER. WHEN THE SYSTEM WAS EVALUATED IT WAS NOTICED THAT THERE ARE TWO CUTS IN THE PROBE CABLE. WHEN THE SYSTEM IS POWERED ON THE END USERS NOTED THAT THERE ARE SEVERAL PRONOUNCED 'STREAKS' IN THE ULTRASOUND IMAGE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7693707 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.