Reported Oct 30, 2024 · Ongoing

Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786; b) REF 1604788; c) REF 1723633

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 Operating table TruSystem 7000 U (MB)
  • Product codes
    • a) REF 1604786
    • b) REF 1604788
    • c) REF 1723633
Lot codes and dates
    • a) REF 1604786
    • UDI/DI 00887761967533
    • b) REF 1604788
    • UDI/DI 00887761967526
    • c) REF 1723633
    • UDI/DI 00887761967519 ALL SERIAL NUMBERS
Amount recalled
6045 units

This recall covers 10 products

The agency filed one notice per product. You are reading one of them; the other 9 are below.

Why it was recalled

The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

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

Want the full recall guide?

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, 5:45 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.