Recall events
/
Event 94777
Event summary
Timeline bucket May 31, 2024
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Siemens Medical Solutions USA, Inc
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
AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395399
Z-2180-2024
Recall number Z-2180-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 50 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2180-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23051]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1003 1032 1039 1060 1065 1071 1076 1082 1083 1085 1089 1092 1104 1170 1174 1181 1183 1194 1304 1305 1309 1310 1315 1318 1323 1325 1331 1348 1359 1382 1395 1398 1423 1443 1444 1447 1449 1452 1453 1468 1498 1500 1508 1509 1512 1513 1515 1516 1525 1531
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[5783]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 9
AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395415
Z-2181-2024
Recall number Z-2181-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 7 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2181-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5583]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1010 1011 1015 1105 1117 1124 1126
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[5411]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 9
AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395381
Z-2182-2024
Recall number Z-2182-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 12 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2182-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10207]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1022 1074 1118 1119 1120 1121 1123 1126 1130 1131 1134 1138
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[5577]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 9
AXIOM MULTIX MP - Inended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395431
Z-2183-2024
Recall number Z-2183-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2183-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5579]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1004 1006 1051 1062 1172 1173 1175 1179 1180 1181 1184 1186 1187 1193 1198 1200 1202 1204 1205 1206
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[5244]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 9
AXIOM Vertix MD - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: MD39543
Z-2184-2024
Recall number Z-2184-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 2 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2184-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29361]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1040 1020
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[5408]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 9
AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: 8627718
Z-2185-2024
Recall number Z-2185-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 4 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2185-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23056]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1004 1006 1011 1014
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[5405]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 9
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517
Z-2186-2024
Recall number Z-2186-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 3 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2186-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10205]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1004 1006 1011 1014
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[5414]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 9
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 475525
Z-2187-2024
Recall number Z-2187-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 3 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2187-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17091]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1523 1585 1897
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[5493]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 9
ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as well as for use in outpatient departments Material Number: 5901900
Z-2188-2024
Recall number Z-2188-2024
Initiated May 31, 2024
Classification Class II
Status Ongoing
Quantity 2 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2188-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5584]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Code information UDI-DI: N/A Serial Numbers: 1239 1241
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[5422]
FDA event record
· Exact recall-number query on openFDA
