Recall events
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Event 83775
Event summary
Timeline bucket August 20, 2019
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Quality Electrodynamics LLC
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
7 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 7
TxRx 15Ch Knee Coil 3T QED part number:Q7000008 Siemens Model # 10185460
Z-0031-2020
Recall number Z-0031-2020
Initiated August 20, 2019
Classification Class II
Status Terminated
Quantity 2 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0031-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50378]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Code information Serial # 1459 1460
Distribution pattern Worldwide distribution - US in the states: NC OUS: Germany
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[29837]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 7
TxRx 15CH Knee Coil 1.5T QED part number:Q7000016 Siemens Model # 10185453
Z-0032-2020
Recall number Z-0032-2020
Initiated August 20, 2019
Classification Class II
Status Terminated
Quantity 3 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0032-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27835]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Code information Serial # 1471 2106 1991
Distribution pattern Worldwide distribution - US in the states: NC OUS: Germany
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[29802]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 7
TxRx CP Extremity Coil 3T QED part number: Q7000019 Siemens Model # 10185464
Z-0033-2020
Recall number Z-0033-2020
Initiated August 20, 2019
Classification Class II
Status Terminated
Quantity 5 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0033-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50371]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Code information Serial # 1308 1309 1310 1311 1313
Distribution pattern Worldwide distribution - US in the states: NC OUS: Germany
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[29298]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 7
TxRx 15CH Knee Coil 1.5T QED part number: Q7000050 Siemens Model # 10606524
Z-0034-2020
Recall number Z-0034-2020
Initiated August 20, 2019
Classification Class II
Status Terminated
Quantity 3 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0034-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3449]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Code information Serial # 1433 1702 1440
Distribution pattern Worldwide distribution - US in the states: NC OUS: Germany
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[29606]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 7
TxRx 15CH Knee Coil 3T QED part number: Q7000051 Siemens Model # 10606525
Z-0035-2020
Recall number Z-0035-2020
Initiated August 20, 2019
Classification Class II
Status Terminated
Quantity 5 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0035-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50372]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Code information Serial # 1571 1572 1573 1574 1575
Distribution pattern Worldwide distribution - US in the states: NC OUS: Germany
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[29242]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 7
TxRx Knee 15 Coil 1.5T QED part number: Q7000056 Siemens Model # 10606828
Z-0036-2020
Recall number Z-0036-2020
Initiated August 20, 2019
Classification Class II
Status Terminated
Quantity 36 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0036-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3441]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Code information Serial # 1694 1841 1887 1933 1998 3195 3291 3292 3293 3294 3298 3299 3300 3301 3302 3303 3304 3305 3306 3307 3308 3309 3310 3311 3312 3313 3314 3315 3316 3317 3318 ¿1137 ¿1361 ¿1378 ¿1628 ¿2447
Distribution pattern Worldwide distribution - US in the states: NC OUS: Germany
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[29939]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 7
TxRx Knee 15 Coil 1.5T QED part number: Q7000057 Siemens Model # 10606829
Z-0037-2020
Recall number Z-0037-2020
Initiated August 20, 2019
Classification Class II
Status Terminated
Quantity 21 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0037-2020
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3434]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
Code information Serial # 1288 1466 2149 2570 2571 2573 2574 2575 2576 2577 2578 2579 2580 2581 2582 2583 2584 2585 ¿1029 1179 ¿1356
Distribution pattern Worldwide distribution - US in the states: NC OUS: Germany
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[29785]
FDA event record
· Exact recall-number query on openFDA
