Device recall: Baxter Operating table column TS7500 MOBIUS, Product Code 1704695
Class II FDA enforcement event 96286. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Baxter Healthcare Corporation started this device recall on 25 Feb 2025. The firm address in the FDA record is in Deerfield, IL. FDA put the recall in Class II. FDA event 96286 has 14 product records. The first FDA enforcement report date is 2 Apr 2025. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
US Nationwide distribution.
Recalling firm
Baxter Healthcare Corporation, Deerfield, IL.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
14 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1409-2025 | Baxter Operating table column TS7500 MOBIUS, Product Code 1704695 | 403 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1410-2025 | Baxter Stationary column TruSystem 7500, Product Code 1717020 | 462 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1411-2025 | Baxter Floor mounting column TruSystem 7500, Product Code 1717021 | 112 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1412-2025 | Baxter Mobile column TruSystem 7500, Product Code 1717023 | 1596 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1413-2025 | Baxter Mobile column TruSystem 7500 U, Product Code 1730720 | 40 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1414-2025 | Baxter Stationary column TruSystem 7500 U, Product Code 1730731 | 2 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1415-2025 | Baxter Floor mounting column TS 7500 U, Product Code 1730732 | 33 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1416-2025 | Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204 | 2 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1417-2025 | Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085 | 10 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1418-2025 | Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086 | 8 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1419-2025 | Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087 | 93 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1420-2025 | Baxter TruSystem 7500 Hybrid Plus (SC), Product Code 1854088 | 48 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1421-2025 | Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886 | 24 units | Class II | Ongoing | 2 Apr 2025 |
| Z-1422-2025 | Baxter TruSystem 7500, Product Code 4091000 | 1709 units | Class II | Ongoing | 2 Apr 2025 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2025
- 945
- Share of these events in Class II
- 85%
- Product records in this event
- 14Median of the firm: 1
- Events of the firm on the register
- 193
Other events of the firm
Official channels
- FDA enforcement report Z-1409-2025The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
Follow by RSS:Food, drug and device recallsFDA Class I recalls
Cite this page
Recall Register. FDA enforcement event 96286. https://recallregister.com/fda/ii/96286/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
US Nationwide distribution.
- What quantity of product is in FDA event 96286?
- The event has 14 product records. The first record gives this quantity:
403 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2025 have the same class?
- 85% of the 945 device events that started in 2025 are in Class II.