FDA recall, , Moderate risk
Baxter TruSystem 7000 U and 7500 U Operating Tables
TruSystem 7000 U Operating Table and Mobile column TruSystem 7500 U may drop unexpectedly, causing patient displacement and serious injury.
Summary by Recall Canary from the FDA notice
What happened
Baxter Healthcare Corporation, of Round Lake, Illinois, voluntarily recalled the TruSystem 7000 U Operating Table (dV), Product Code 1723633, and the Mobile column TruSystem 7500 U, Product Code 1730720. The recall was initiated on September 14, 2026, and was added to the FDA's Enforcement Report on November 3, 2026.
The main lift may unexpectedly drop from its set position to its lowest position during use, and the tabletop may not be able to be raised again after the drop occurs.
An uncontrolled drop of the surgical table may result in an abrupt patient displacement during surgery, potentially leading to serious or critical adverse health consequences, including traumatic injury, airway compromise, and surgical procedure complications.
The products were distributed nationwide in the states of Illinois, Missouri, and Texas. Baxter notified customers by letter.
What to do
The FDA notice gives no instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
2 products
Match the UDI-DI and serial number listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
TruSystem 7000 U Operating Table (dV), Product Code 1723633
- UDI-DI
- 00887761967519
- Serial number
- 110188921
- 110188922
- 110206662
Mobile column TruSystem 7500 U, Product Code 1730720
- UDI-DI
- 00887761974388
- Serial number
- 110183858
Recall details
- Posted by FDA
- Recall began
- Status
- Open
- Weekly archive
- Listed the week of Nov 2, 2026
- Recalled by
- Baxter Healthcare CorporationRound Lake, Illinois
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- FDA event number
- 99826
- Recall numbers
- Z-0332-2027 to Z-0333-2027
- Recall type
- Voluntary: Firm initiated
- How the company first told customers
- Letter
All recalls from Baxter Healthcare Corporation
Timeline
FDA's Enforcement Report is its public list of recalls; FDA posts a recall by adding it there.
Baxter Healthcare began the recall
FDA posted the recall to its Enforcement Report and rated it Class II (moderate risk)
Added to Recall Canary
