Recall events
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Event 95409
Event summary
Timeline bucket September 19, 2024
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
9 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 9
Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786; b) REF 1604788; c) REF 1723633
Z-0210-2025
Recall number Z-0210-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity 6045 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0210-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28657]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information a) REF 1604786, UDI/DI 00887761967533; b) REF 1604788, UDI/DI 00887761967526; c) REF 1723633, UDI/DI 00887761967519 ALL SERIAL NUMBERS
Distribution pattern Worldwide 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[4057]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 9
Baxter Operating Table TruSystem 7000, Product code REF 1841046
Z-0211-2025
Recall number Z-0211-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity 397 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0211-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32682]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information UDI/DI 00887761968714, All Serial Numbers
Distribution pattern Worldwide 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[4835]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 9
Baxter Operating Table TruSystem 7000 (MBW), Product code REF 1841048
Z-0212-2025
Recall number Z-0212-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0212-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40738]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information UDI/DI 00887761968714, All Serial Numbers
Distribution pattern Worldwide 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[4143]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 9
Baxter Operating Table TruSystem 7000 (dV), Product code REF 1841049
Z-0213-2025
Recall number Z-0213-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity 1077 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0213-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52461]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information UDI/DI00887761968691, All Serial Numbers
Distribution pattern Worldwide 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[4564]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 9
Baxter Operating Table TruSystem 7000 V, Product code REF 1841050
Z-0214-2025
Recall number Z-0214-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity 4 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0214-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46927]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information UDI/DI 00887761974241, All Serial Numbers
Distribution pattern Worldwide 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[4124]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 9
Baxter Operating Table TruSystem 7000 (MBW) V, Product code REF 1841082
Z-0215-2025
Recall number Z-0215-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity 24 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0215-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23142]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information UDI/DI 00887761974234, All Serial Numbers
Distribution pattern Worldwide 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[4540]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 9
Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083
Z-0216-2025
Recall number Z-0216-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0216-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17334]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information UDI/DI 00887761974227, All Serial Numbers
Distribution pattern Worldwide 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[4363]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 9
Baxter Operating Table TruSystem 7000 U14 (MBW), Product code REF 2065385
Z-0217-2025
Recall number Z-0217-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity 542 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0217-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40739]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information UDI/DI 00887761968653, All Serial Numbers
Distribution pattern Worldwide 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[4232]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 9
Baxter Operating Table TruSystem 7000 U14 (MBW) V, Product code REF 2065386
Z-0218-2025
Recall number Z-0218-2025
Initiated September 19, 2024
Classification Class II
Status Ongoing
Quantity 13 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0218-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32684]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Code information UDI/DI 00887761973794, All Serial Numbers
Distribution pattern Worldwide 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[4082]
FDA event record
· Exact recall-number query on openFDA
