# FDA recall Z-2512-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2024-06-28.

## Product

Baxter PST 500 U, Precision Surgical Table, Part number (product code) 4080300

## Reason for recall

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.

## Distribution

Worldwide distribution - US Nationwide and the country of Canada.

## Key facts

- **Recall number:** Z-2512-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-28
- **Report date:** 2024-08-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2512-2024

## Citation

> AI Analytics. FDA recall Z-2512-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2512-2024. Source: US FDA. Licensed CC0.

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