ALLENRecalls & reported problems across all models
Hill-Rom, Inc. · 24 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one ALLEN model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 73
- Deaths reported
- 0
- Injuries reported
- 13
- Recalls
- 5
We found 24 models of ALLEN by Hill-Rom, Inc. in the FDA's device registry (GUDID). Together they are named in 73 adverse event reports in the FDA's MAUDE database, received between Mar 25, 2020 and Sep 25, 2026 — classified as 13 injuries, 60 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (23 reports).
5 FDA recall records name at least one of these models by its device identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
ALLEN recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Feb 14, 2024Open, Classified
Three lots of the Boot Assembly, Traction Device are being recalled due to due to a customer report of an incorrectly oriented locking pin which caused the boot to detach from the traction system. If an impacted device is used during surgery, the boot may detach from the traction system, potentially leading to patient harm and a delay in surgery.
Z-1289-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- May 18, 2023Open, Classified
Potential for the device to crack where the Chest Base Prone support attaches to the carbon fiber operating room (OR) table rail.
Z-2109-2023 · Root cause: Device Design · Recall details · FDA record ↗
- Sep 20, 2022Terminated
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.
Z-0179-2023 · Root cause: Other · Recall details · FDA record ↗
- Sep 20, 2022Terminated
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.
Z-0176-2023 · Root cause: Other · Recall details · FDA record ↗
- Sep 20, 2022Terminated
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.
Z-0175-2023 · Root cause: Other · names 2 of these models · Recall details · FDA record ↗
Most reported ALLEN problems
Device problems
- Unintended Movement23
- Fracture10
- Positioning Failure9
- Positioning Problem8
- Device Fell7
- Manufacturing, Packaging or Shipping Problem3
- Mechanical Problem3
- Detachment of Device or Device Component2
Patient problems
- No Clinical Signs, Symptoms or Conditions58
- Nerve Damage4
- Numbness3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
- Laceration(s)2
- Pain2
- Pressure Sore/Ulcer2
- Ambulation or Postural Difficulties1
ALLEN models
24 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ALLEN 103001SUPPORT, PATIENT POSITION1 recall17 reports
- ALLEN 107003Table, operating-room, electrical1 recall9 reports
- ALLEN 104002Operating Room Accessories Table Tray1 recall8 reports
- ALLEN 107004Operating Room Accessories Table Tray1 recall5 reports
- ALLEN 108001Operating Room Accessories Table Tray1 recall3 reports
- ALLEN 107003Table, operating-room, electrical1 recall0 reports
- ALLEN 102001Operating Room Accessories Table Tray7 reports
- ALLEN 107003Table, operating-room, electrical3 reports
- ALLEN 107004Operating Room Accessories Table Tray2 reports
- ALLEN 102001Operating Room Accessories Table Tray2 reports
- ALLEN 102001Operating Room Accessories Table Tray2 reports
- ALLEN 102001Operating Room Accessories Table Tray2 reports
- ALLEN 102001Operating Room Accessories Table Tray2 reports
- ALLEN 102001Operating Room Accessories Table Tray1 report
- ALLEN 102001Operating Room Accessories Table Tray1 report
- ALLEN 101001Operating Room Accessories Table Tray1 report
- ALLEN 103003Operating Room Accessories Table Tray1 report
- ALLEN 103001SUPPORT, PATIENT POSITION1 report
- ALLEN 107003Table, operating-room, electrical1 report
- ALLEN 107003Table, operating-room, electrical1 report
- ALLEN 107003Table, operating-room, electrical1 report
- ALLEN 102001Operating Room Accessories Table Tray1 report
- ALLEN 102001Operating Room Accessories Table Tray1 report
- ALLEN 102001Operating Room Accessories Table Tray1 report
Recent ALLEN adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50901665 ↗MalfunctionSep 25, 2026Device Fell
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50898027 ↗MalfunctionSep 9, 2026Device Fell
Baxter received a report that YELLOFINS APEX STRUP PAIR had the stirrup dropped unexpectedly . There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50681355 ↗MalfunctionAug 27, 2026Device Dislodged or Dislocated
Baxter received a report that ALLEN YELLOFIN ELITE had stirrup does not stay tight. This occurred before use. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50465739 ↗MalfunctionAug 25, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50442154 ↗MalfunctionAug 25, 2026Device Fell
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50438959 ↗MalfunctionAug 25, 2026Positioning Problem; Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50438012 ↗MalfunctionAug 18, 2026Device Slipped
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50312230 ↗MalfunctionAug 13, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50241199 ↗MalfunctionAug 12, 2026Unintended Movement
Baxter received a report that advance rail top had rail top attachment not holding in place. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50217131 ↗MalfunctionAug 11, 2026Unintended Movement
Baxter received a report that ALLEN ADVANCE TABLE US had brakes not holding. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50216849 ↗MalfunctionAug 6, 2026Collapse
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50158606 ↗MalfunctionJul 28, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50060158 ↗MalfunctionJul 17, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25855058 ↗MalfunctionJun 11, 2026Unstable
BAXTER RECEIVED A REPORT THAT ALLEN ADVANCE TBL THE THIGH AND HIP SECTIONS EXHIBIT MOVEMENT EVEN WHEN LOCKED . THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25477859 ↗
Other Hill-Rom, Inc. products
- Centrella Bed2 models · 2,021 reports · 2 recalls
- VersaCare Med Surg Bed2 models · 1,200 reports
- pro+18 models · 36 reports · 13 recalls
- Voalte Nurse Call2 models · 419 reports · 2 recalls
- WatchCare4 models · 0 reports · 4 recalls
- NaviCare Nurse Call Systems3 models · 99 reports · 2 recalls
- CompellaSurface3 models · 87 reports · 1 recall
- Progressa Surface13 models · 8 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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