ALLEN 107004 (REF F-71305)Recalls & reported problems
Hill-Rom, Inc. · Advance Hip Support - MED w/pad · Class 1
All models of ALLEN (24)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00615521013196), received between Mar 24, 2021 and Mar 24, 2021 — classified as 2 injuries.
The most frequently reported specific device problem is “Difficult or Delayed Positioning” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Difficult or Delayed Positioning2
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 24, 2021Difficult or Delayed Positioning; Difficult or Delayed Positioning
THE CUSTOMER REPORTED THAT INCREASED PRESSURE IN THE CHEST OF THE PATIENT AFTER SURGERY LED TO POTASSIUM LEVEL ELEVATION AND RHABDOMYOLYSIS. THIS EVENT STEMS FROM A USER INCIDENT REPORT NOTIFIED TO HILLROM (VIA DISTRIBUTOR DICO) BY THE (B)(4) MEDICINES AGENCY ON 10 NOV 2020. HILLROM HAS LOGGED A COMPLAINT AND DETERMINED THAT THIS IS A REPORTABLE EVENT UNDER CURRENT REGULATIONS.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11565046 ↗InjuryMar 24, 2021Difficult or Delayed Positioning; Difficult or Delayed Positioning
THE CUSTOMER REPORTED THAT THE SURGEON IS DETECTING HIGH KALIUM VALUES ON THE PATIENT. THE CUSTOMER REPORTS THAT THE PATIENTS HAS TOO HIGH PRESSURE ON THEIR CHEST DURING THE OPERATION. THEY FEEL THE CHEST IS TOO LOW COMPARED WITH THE HIP POSITIONING, AND DUE TO THIS, THE PRESSURE ON THE CHEST IS RAISING DURING THE SURGERY. THIS EVENT STEMS FROM A USER INCIDENT REPORT NOTIFIED TO HILLROM (VIA DISTRIBUTOR (B)(4)) BY THE (B)(6) ON 10 NOV 2020. HILLROM HAS LOGGED A COMPLAINT ((B)(4)) AND DETERMINED THAT THIS IS A REPORTABLE EVENT UNDER CURRENT REGULATIONS.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11564653 ↗
Other Operating Room Accessories Table Tray devices
- MAYFIELD® A2101Integra Lifesciences Corporation · Operating Room Accessories Table Tray101 reports
- NA 210080Mako Surgical Corp. · Operating Room Accessories Table Tray74 reports
- ALLEN 104002Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall8 reports
- N/A 7210569Smith & Nephew, Inc. · Accessories, operating-room, table (kit)57 reports
- ALLEN 107004Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall5 reports
- ALLEN 108001Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall3 reports
- NA 7210551Smith & Nephew, Inc. · Accessories, operating-room, table (kit)41 reports
- MAYFIELD® A1018Integra Lifesciences Corporation · Operating Room Accessories Table Tray36 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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