Recall events
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Event 96286
Event summary
Timeline bucket February 25, 2025
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Baxter Healthcare Corporation
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
14 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 14
Baxter Operating table column TS7500 MOBIUS, Product Code 1704695
Z-1409-2025
Recall number Z-1409-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 403 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1409-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32732]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974425, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38266]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 14
Baxter Stationary column TruSystem 7500, Product Code 1717020
Z-1410-2025
Recall number Z-1410-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 462 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1410-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11493]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974418, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37750]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 14
Baxter Floor mounting column TruSystem 7500, Product Code 1717021
Z-1411-2025
Recall number Z-1411-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 112 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1411-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5654]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974401, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37979]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 14
Baxter Mobile column TruSystem 7500, Product Code 1717023
Z-1412-2025
Recall number Z-1412-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 1596 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1412-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32733]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974395, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37985]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 14
Baxter Mobile column TruSystem 7500 U, Product Code 1730720
Z-1413-2025
Recall number Z-1413-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 40 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1413-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5653]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974388, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38251]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 14
Baxter Stationary column TruSystem 7500 U, Product Code 1730731
Z-1414-2025
Recall number Z-1414-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 2 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1414-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46961]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974371, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38324]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 14
Baxter Floor mounting column TS 7500 U, Product Code 1730732
Z-1415-2025
Recall number Z-1415-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 33 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1415-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17186]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974364, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38498]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 14
Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204
Z-1416-2025
Recall number Z-1416-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 2 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1416-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5656]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974326, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38489]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 14
Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085
Z-1417-2025
Recall number Z-1417-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 10 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1417-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5661]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974081, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38319]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1418-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 8 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1418-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17172]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974074, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37898]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1419-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 93 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1419-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40320]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974067, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38301]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1420-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 48 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1420-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11501]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761974050, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37976]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1421-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 24 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1421-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29014]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761973763, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38334]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1422-2025
Initiated February 25, 2025
Classification Class II
Status Ongoing
Quantity 1709 units
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1422-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11499]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Code information UID/DI 00887761968639, All serial numbers manufactured until 11/14/2024.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38315]
FDA event record
· Exact recall-number query on openFDA
