ALLEN 107003 (REF A-71101-SK)Recalls & reported problems
Hill-Rom, Inc. · Allen Advance Table · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00615521003081), received between Feb 5, 2026 and Feb 5, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 5, 2026Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT STABILIZER LEG HDS HAD BRAKES NOT HOLDING. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24271639 ↗
Other Table, operating-room, electrical devices
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- TS 7000 1723633Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall22 reports
- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall9 reports
- Head-Positioning accessories 1739994Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall1 report
- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall0 reports
- TS 7500 4091000Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- TS 7500 1717021Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- TS 7500 2067886Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.