CLASS II ONGOING Device recall · Reported 30 Oct 2024 · FDA Enforcement Report

Baxter Operating table TruSystem 7000 U (MB), Product codes: a) recalled

Baxter Healthcare is recalling Baxter Operating table TruSystem 7000 U (MB), Product codes: a). The recall was initiated on 19 Sep 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesa) REF 1604786, UDI/DI 00887761967533; b) REF 1604788, UDI/DI 00887761967526; c) REF 1723633, UDI/DI 00887761967519 ALL SERIAL NUMBERS

Quantity recalled6045 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0210-2025
FDA event ID: 95409
Recalling firm: Baxter Healthcare, Deerfield, IL
Classification: Class II
Status: Ongoing
Recall initiated: 19 Sep 2024
FDA classified: 24 Oct 2024
Reported: 30 Oct 2024
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

19 Sep 2024	Recall initiated by company
24 Oct 2024	Classified by FDA	+35 days
30 Oct 2024	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

Worldwide distribution.

Questions about this recall

Is Baxter Operating table TruSystem 7000 U (MB), Product codes: a) recalled?

Yes. Baxter Healthcare recalled Baxter Operating table TruSystem 7000 U (MB), Product codes: a) on 19 Sep 2024. The recall is Class II and its status is Ongoing. Recall number Z-0210-2025.

Why was it recalled?

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

Which lots are affected?

a) REF 1604786, UDI/DI 00887761967533; b) REF 1604788, UDI/DI 00887761967526; c) REF 1723633, UDI/DI 00887761967519 ALL SERIAL NUMBERS

Where was it sold?

Worldwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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