Recall events
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Event 72202
Event summary
Timeline bucket October 06, 2014
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording MWT Materials, 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
11 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 11
Accusorb MRI MAC7001 Part Number: MRI-01 MRI-Large Blanket Various Sizes Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0663-2016
Recall number Z-0663-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 49 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0663-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[14709]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[17992]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 11
Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0664-2016
Recall number Z-0664-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 31 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0664-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[49961]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[19840]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 11
Accusorb MRI MAC7004 Part Number: MRI-04 MRI-Poncho Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0665-2016
Recall number Z-0665-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity one unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0665-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[55914]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[18113]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 11
Accusorb MRI MAC7007 Part Number: MRI-07 MRI-Breast Shield Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0666-2016
Recall number Z-0666-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 6 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0666-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[2929]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[18640]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 11
Accusorb MRI MAC7008 Part Number: MRI-08 MRI-Boot Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0667-2016
Recall number Z-0667-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 15 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0667-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[55917]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[22538]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 11
Accusorb MRI MAC7003 Part Number: MRI-03 U (Upper) and MRI-03 L (Lower) Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0668-2016
Recall number Z-0668-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 14 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0668-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[8901]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[25525]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 11
Accusorb MRI MAC7005 Part Number: MRI-05 Leg Wrap Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0669-2016
Recall number Z-0669-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 18 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0669-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[14710]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[22591]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 11
Accusorb MRI MAC7006 Part Number: MRI-06 MRI-Large Torso Wrap Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0670-2016
Recall number Z-0670-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 5 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0670-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32541]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[25476]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 11
Accusorb MRI MAC7009 Part Number: MRI-09 MRI- Leg Wrap Blanket Various Sizes Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Z-0671-2016
Recall number Z-0671-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 47 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0671-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32525]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[22571]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0672-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 1 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0672-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[36592]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[24755]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0673-2016
Initiated October 06, 2014
Classification Class II
Status Terminated
Quantity 1 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0673-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32524]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
Distribution pattern US Nationwide Distribution in the states of NY and MA.
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[18301]
FDA event record
· Exact recall-number query on openFDA
