Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2512-2024 — Baxter PST 500 U, Precision Surgical Table, Part number (product code) 4080300

U.S. FDA — Device Enforcement · United States · 2024-06-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2512-2024
Date of alert
2024-06-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00887761973671
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.