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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 2 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. 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

All Table, radiologic devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.