Reported Aug 14, 2024 · Ongoing

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

Baxter Healthcare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

    • Baxter PST 500 U
    • Precision Surgical Table
    • Part number (product code) 4080300
Lot codes and dates
  • UDI/DI 00887761973671
  • Serial Numbers

    400 of 400 codes

    • 107936298
    • 107936299
    • 107936300
    • 107946575
    • 107946576
    • 107949857
    • 107951075
    • 107952514
    • 107954982
    • 108021169
    • 108023287
    • 108028575
    • 108028716
    • 108028747
    • 108028798
    • 108028801
    • 108028803
    • 108028817
    • 108028829
    • 108028840
    • 108028846
    • 108029046
    • 108029052
    • 108029053
    • 108049023
    • 108049024
    • 108049948
    • 108049950
    • 108049955
    • 108049967
    • 108050823
    • 108050824
    • 108055575
    • 108055576
    • 108055577
    • 108055581
    • 108123400
    • 108127380
    • 108129826
    • 108129828
    • 108131719
    • 108131745
    • 108133272
    • 108133273
    • 108160433
    • 108160447
    • 108160448
    • 108160452
    • 108160453
    • 108160454
    • 108160455
    • 108167451
    • 108167552
    • 108167553
    • 108167554
    • 108167561
    • 108167597
    • 108167598
    • 108167701
    • 108167702
Amount recalled
400 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:59 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.