ALLEN 102001 (REF O-YFES-L)Recalls & reported problems
Hill-Rom, Inc. · LEFT - Allen Yellofin Elite · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00615521020156), received between Jul 19, 2021 and Jul 28, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (2 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
- Unintended Movement2
- Mechanical Jam1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 28, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50060158 ↗InjuryJul 19, 2021Mechanical Jam; Unintended Movement; Mechanical Jam; Unintended Movement
HILLROM RECEIVED A REPORT THAT THE YELLOFINS STIRRUP WAS NOT FUNCTIONING PROPERLY AND DURING USE, THE STIRRUP SHOT UP AND HIT A NURSE IN THE FACE. THE DEVICE WAS LOCATED AT THE ACCOUNT. THERE WAS USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: Insufficient Information
MAUDE report 12193061 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.