FDA recall, , Moderate risk
Baxter TruSystem 7500 and TruSystem 7000 U Surgical Tables
TruSystem surgical tables and operating table columns may drop unexpectedly, causing abrupt patient displacement during surgery.
Summary by Recall Canary from the FDA notice
What happened
Baxter Healthcare Corporation of Deerfield, Illinois, voluntarily recalled multiple TruSystem surgical tables and operating table columns due to an issue with the main lift mechanism. The main lift may unexpectedly drop from its set position to its lowest position during use, and in these cases, the tabletop could not be raised again after the drop occurred. The issue has been associated with unexpected wear of the main lift assembly, also known as the telescopic spindle.
The recall includes the Operating Table TruSystem 7000 U, Operating table column TS7500 MOBIUS, TruSystem 7500 surgical table, TruSystem 7500 Hybrid Plus (FC), and Operating Table TruSystem 7000 U (dV). The company began the recall on September 29, 2026, and the FDA added it to the Enforcement Report on November 3, 2026. Distribution was nationwide in the US.
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?
5 products
Match the UDI-DI, serial number and catalog code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Operating Table TruSystem 7000 U, Surgical table, universal, Model/
- UDI-DI
- 00887761967526
- Catalog code
- 1604788
- Serial number
- 108517025
- 110115554
- 110144247
- 110188916
- 109558596
- 110139748
- 110166201
- 110188918
- 109737582
- 110139769
- 110177678
- 110192686
- 110115551
- 110144245
- 110185616
- 109889060
Operating table column TS7500 Mobius, Hybrid operating table column, Model/
- UDI-DI
- 00887761974425
- Catalog code
- 1704695
- Serial number
- 108094281
- 108468075
- 108484417
- 108506318
- 108516636
- 108536785
- 108544115
- 108604154
- 108463223
- 108484404
- 108489634
- 108511411
- 108516637
- 108544106
- 108544116
- 108618964
- 108463224
- 108484405
- 108489648
- 108511412
- 108521436
- 108544107
- 108604137
- 108618965
- 108468062
- 108484406
- 108506316
- 108511413
- 108521452
- 108544110
- 108604140
- 108468063
- 108484408
- 108506317
- 108516634
- 108536776
- 108544111
- 108604153
TruSystem 7500 surgical table, Model/
- UDI-DI
- 00887761968639
- Catalog code
- 4091000
- Serial number
- 108491706
- 108726496
- 108758657
- 108858029
- 108945825
- 109083212
- 109343910
- 109684319
- 110016886
- 108557062
- 108736192
- 108773032
- 108882327
- 108976094
- 109174333
- 109370104
- 109690845
- 110016887
- 108574826
- 108736193
- 108773033
- 108882328
- 108976095
- 109174334
- 109396256
- 109690846
- 110072583
- 108578755
- 108736194
- 108842519
- 108883564
- 108976101
- 109174335
- 109464647
- 109708813
- 110084982
- 108580717
- 108736195
- 108842523
- 108883565
- 109047445
- 109174336
- 109464648
- 109708816
- 110086138
- 108580718
- 108743656
- 108842524
- 108896687
- 109047446
All 129
- 109228237
- 109464649
- 109885369
- 110144223
- 108580720
- 108743657
- 108842525
- 108896688
- 109047447
- 109228238
- 109464650
- 109896735
- 110144224
- 108604827
- 108745163
- 108842526
- 108912913
- 109047448
- 109249973
- 109488031
- 109896736
- 110144225
- 108604828
- 108745164
- 108842679
- 108912914
- 109047451
- 109249974
- 109493243
- 109896737
- 110158878
- 108604832
- 108745165
- 108842680
- 108931731
- 109047452
- 109249989
- 109500155
- 109896738
- 110158879
- 108604833
- 108745166
- 108849690
- 108931732
- 109047460
- 109301944
- 109561673
- 109933665
- 110175899
- 108726492
- 108745180
- 108849691
- 108945772
- 109047461
- 109301945
- 109561674
- 109948691
- 110175900
- 108726493
- 108745181
- 108849694
- 108945823
- 109078531
- 109301946
- 109571317
- 110007863
- 110163294
- 108726495
- 108758656
- 108849695
- 108945824
- 109078533
- 109343482
- 109571318
- 110016883
- 110163293
- 110183861
- 110220396
- 110220395
TruSystem 7500 Hybrid Plus (FC), Fixed-Installation Operating Table Column, Model/
- UDI-DI
- 00887761974067
- Catalog code
- 1854087
- Serial number
- 107971925
Operating Table TruSystem 7000 U (dV), Model/
- UDI-DI
- 00887761967519
- Catalog code
- 1723633
- Serial number
- 108920104
- 110192607
- 110192885
- 110208936
- 110212885
- 110220066
- 110227520
- 110248337
- 110250614
- 109423464
- 110192608
- 110192886
- 110208941
- 110212886
- 110220068
- 110227523
- 110248343
- 110250621
- 109517138
- 110192609
- 110206656
- 110210717
- 110220055
- 110220069
- 110227524
- 110249706
- 110250622
- 110139767
- 110192683
- 110206657
- 110210718
- 110220056
- 110220071
- 110227525
- 110249712
- 110206662
- 110139776
- 110192882
- 110206659
- 110210720
- 110220057
- 110220072
- 110227552
- 110250605
- 110188921
- 110188919
- 110192883
- 110206660
- 110210721
- 110220058
All 62
- 110220078
- 110227553
- 110250609
- 110188922
- 110188920
- 110192884
- 110206664
- 110212881
- 110220065
- 110220079
- 110248218
- 110250613
Recall details
- Posted by FDA
- Recall began
- Status
- Open
- Weekly archive
- Listed the week of Nov 2, 2026
- Sold in
Worldwide - US Nationwide distribution.
- Recalled by
- Baxter Healthcare CorporationDeerfield, 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
- 100117
- Recall numbers
- Z-0350-2027 to Z-0354-2027
- 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
