Orthopedic Extension 1232546Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · Leather extension sandal right · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00887761972513), received between May 20, 2025 and May 20, 2025 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 20, 2025Unintended Movement; Unintended Movement
IT WAS INITIALLY REPORTED BY THE BAXTER DISTRIBUTOR IN ISRAEL THAT DURING THE USE OF THE LEATHER EXTENSION SANDAL ACCESSORY USE WITH A P500 SURGICAL TABLE, THE PATIENTS LEG SLIPPED OFF THE SANDAL DURING THE PROCEDURE. IT IS UNKNOWN IF AN INJURY OCCURRED WITH THIS EVENT AS THERE WAS NO REPORT OF INJURY IN THE INITIAL REPORT. FOLLOW-UP COMMUNICATION WITH THE COMPLAINANT FOUND THAT THE COMPLAINANT COULD NOT PROVIDE ANY ADDITIONAL DETAILS OF THE EVENT, COULDN¿T CONFIRM IF AN INJURY OCCURRED, NOR HAD ANY DETAILS OF ANY INJURY.
Patient problems: Insufficient Information
MAUDE report 22051506 ↗
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- TS 7500 1717021Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
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- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall0 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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