PST500 4080300Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · PST 500 U · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887761973671), received between Jun 26, 2025 and Feb 19, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (2 reports).
1 FDA recall record name this device's identifier, 1 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, 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
Recalls naming this device
- Jun 28, 2024Open, Classified
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the PST 500 U Precision Surgical Table due to a potential issue with loose spring pins in the spindle drives. This can cause the tabletop to unexpectedly tilt or move at any time, even without active use of the surgical table. This could potentially result in unintentional patient movement during surgical procedures and/or preparation for surgical procedures, including transport.
Z-2512-2024 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Unintended Movement2
- Device Slipped1
- Unstable1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 19, 2026Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT PST 500 U HAD 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 24393160 ↗MalfunctionNov 24, 2025Device Slipped; Device Slipped
BAXTER RECEIVED A REPORT STATING THAT PST 500 U MAIN PAD SLID AWAY FROM TABLETOP WHEN THE TABLE WAS IN TRENDLEBURG POSITION. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23639302 ↗MalfunctionNov 21, 2025Unstable; Unstable
BAXTER RECEIVED A REPORT STATING THAT PST 500 U LEFT LEG JACKING CYLINDER AND CASTER DETACHED FROM TABLE BASE CHASIS. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23619547 ↗MalfunctionJun 26, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT PST 500 U TABLE WAS GOING DOWN BY ITSELF. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO INJURY, DEATH, OR PROCEDURAL DELAY REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22336615 ↗
Other Table, radiologic devices
- ORT300 TableIMRIS Imaging, Inc. · Table, Radiologic2 recalls6 reports
- NA 6265300GE Medical Systems, L.L.C. · Table, radiologic2 recalls0 reports
- TS 7500 1730720Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall1 report
- TS 7500 1730731Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- TS 7500 1854086Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- NA 6265300-20GE Medical Systems, L.L.C. · Table, radiologic1 recall0 reports
- TS 7000 1604786Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- TS 7500 1854088Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.