Exact FDA event identifier

Event 84585

6 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: November 24, 2019
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Microvention, 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

6 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 6

Terumo AZUR Peripheral Coil System, Detachable 18, Helical HydroCoil Embolization System, REF numbers 45-481015, 45-481020, 45-481215, 45-481220, 45-481515, 45-481520, 45-482020, 45-482030, 45-480202, 45-480204, 45-480310, 45-480302, 45-480305, 45-480410, 45-480415, 45-480420, 45-480405, 45-480610, 45-480615, 45-480620, 45-480815, 45-480820, MV-AZ80520HL, MV-AZ80202HL, MV-AZ80204HL, MV-AZ80305HL, MV-AZ80310HL, MV-AZ80410HL, MV-AZ80420HL, MV-AZ80620HL, MV-AZ80820HL, and MV-AZ81020HL, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.

Z-1220-2020

Recall number: Z-1220-2020
Initiated: November 24, 2019
Classification: Class II
Status: Terminated
Recalling firm: Microvention, Inc.
Quantity: 445 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The devices may be missing the implant coil.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The devices may be missing the implant coil.

Code information

Catalog/lot numbers: 45-481015 - 19031155A; 45-481020 - 19031355E and 190424567; 45-481215 - 19031154K and 19041554Z; 45-481220 - 19051357G; 45-481515 - 19041554W and 19041556Q; 45-481520 - 19032053A; 45-482020 - 190320539 and 19040855Y; 45-482030 - 19040855X; 45-480202 - 19032054J and 190506581; 45-480204 - 19051357N; 45-480310 - 19031154N, 19031355G, 190401554, and 19050657X; 45-480302 - 19050657V and 19051357P; 45-480305 - 19031154L, 19031354G, 19031355F, 19042254K, 19042453J, 19050657W, and 19051357L; 45-480410 - 19031154G,19031155B, 19031354H, 19031355H, 19032054N, 190415553, 19042254L, and 19051357K; 45-480415 - 19041554V and 19050657U; 45-480420 - 190506582 and 19051357H; 45-480405 - 190424568; 45-480610 - 19041554Y, 19041556V, and 19051357J; 45-480615 - 19042254G; 45-480620 - 19031354J, 19041554X, and 19042453K; 45-480815 - 19040853U and 190415552; 45-480820 - 19031355J,19032053C, and 19032252U; MV-AZ80520HL - 190401556, 190401566, and 19040554H; MV-AZ80202HL - 190517542 and 190517566; MV-AZ80204HL - 19051756C; MV-AZ80305HL - 190517543; MV-AZ80310HL - 190517544; MV-AZ80410HL - 19040554J and 19040555X; MV-AZ80420HL - 19050253Y, 19050254W, 190517545, and 190517569; MV-AZ80620HL - 19050254V and 190517546; MV-AZ80820HL - 19051756A; and MV-AZ81020HL - 190517564.

Distribution pattern

The devices were distributed to Maryland. There was no direct military/government distribution. Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico.

device · product 2 of 6

Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil, REF numbers 45-681026, 45-681434, 45-682050, and 45-680820, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.

Z-1221-2020

Recall number: Z-1221-2020
Initiated: November 24, 2019
Classification: Class II
Status: Terminated
Recalling firm: Microvention, Inc.
Quantity: 107 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The devices may be missing the implant coil.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The devices may be missing the implant coil.

Code information

Catalog/lot numbers: 45-681026 - 1903085J5,1903155J5, and 1904035J5; 45-681434 - 1903015J5,1903155J5, and 1904155J5; 45-682050 - 1903085K5, 1903135J5, 1903155J5, 1904015J5, 1904155J5, 1904175J5, and 1905105K5; and 45-680820 - 1903045J5, 1903085K5, 1903155J5, 1904015J5, 1904035J5, and 1904155J5.

Distribution pattern

The devices were distributed to Maryland. There was no direct military/government distribution. Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico.

device · product 3 of 6

Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers 45-781032, 45-781238, 45-781434, 45-781639, 45-781836, 45-782040, 45-780202, 45-780204, 45-780304, 45-780308, 45-780413, 45-780516, 45-780620, 45-780724, 45-780828, 45-780928, MV-AX80202CL, MV-AX80204CL, MV-AX80304CL, MV-AX80308CL, MV-AX80413CL, MV-AX80516CL, MV-AX80620CL, MV-AX80724CL, MV-AX80828CL, MV-AX80928CL, MV-AX81032CL, MV-AX81238CL, MV-AX81434CL, MV-AX81639CL, and MV-AX82040CL, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.

Z-1222-2020

Recall number: Z-1222-2020
Initiated: November 24, 2019
Classification: Class II
Status: Terminated
Recalling firm: Microvention, Inc.
Quantity: 3,881 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The devices may be missing the implant coil.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The devices may be missing the implant coil.

Code information

Catalog/lot numbers: 45-781032 - 1903065Z8,1903085Z8, 1903155Z8, 1903205Z8, 1903225Z8, 1904015Z8, 1904055Z8, 1904085Z8, 1904155Z8, 1904245Z8, 1904265Z8, 1904295Z8, and 1905155Z8; 45-781238 - 1903115Z8, 1903135Z8, 1903205Z8, 1904105Z8, 1904155Z8, 1904295Z8, and 1905065Z8; 45-781434 - 1903115Z8, 1903155Z8, 1904015Z8, 1904105Z8, 1904155Z8, and 1905155Z8; 45-781639 - 1903155Z8, 1903185Z8, and 1904015Z8; 45-781836 - 1903065Z8, 1903115Z8, 1903205Z8, 1903225Z8, 1904015Z8, 1904085Z8, 1904155Z8, and 1905155Z8; 45-782040 - 1903045Z8, 1903115Z8, 1903185Z8, 1904015Z8, 1904055Z8, 1904155Z8, 1905035ZA, 1905065Z8, 1905085Z8, and 1905155Z8; 45-780202 - 1903115Z8, 1903135Z8, 1903185Z8, 1904055Z8, 1904085Z8, 1904175ZA, 1904225Z8, 1904245Z8, 1904265Z8, 1904295Z8, 1905135Z8, and 1905205Z8; 45-780204 - 1903045Z8, 1903085Z8, 1903115Z8, 1903135Z8, 1904015Z8, 1904035Z8, 1904085Z8, 1904105Z8, 1904155Z8, 1904175Z8, 1904225Z8, 1904245Z8, 1904265Z8, 1904295Z8,1905025Z8, 1905035Z8, 1905065Z8, 1905085Z8, 1905105Z8, 1905105ZA, 1905135Z8, and 1905205Z8; 45-780304 - 1903085Z8, 1903115Z8, 1903135Z8, 1903135ZA, 1904035Z8, 1904035ZA, 1904175Z8, 1904175ZA, 1904225Z8, 1904245Z8, and 1904265Z8; 45-780308 - 1903015Z8, 1903045Z8, 1903115Z8, 1903135Z8, 1903155Z8, 1903185Z8, 1904055Z8, 1904105Z8, 1904155Z8, 1904175Z8, 1904225Z8, 1904245Z8, 1904265Z8, 1904295Z8, 1905035Z8, 1905065Z8, 1905085Z8, 1905135Z8, and 1905205Z8; 45-780413 - 1903015Z8, 1903045Z8,1903115Z8, 1903135Z8, 1903135ZA, 1903155Z8, 1904105Z8, 1904155Z8, 1904175Z8, 1904225Z8, 1904265Z8, 1904295Z8, 1905025Z8, 1905085Z8, 1905105Z8, 1905135Z8, and 1905205Z8; 45-780516 - 1903045Z8, 1903115Z8, 1903135Z8, 1903205Z8, 1904055Z8, 1904085Z8, 1904225Z8, 1904265Z8, 1904295Z8, 1905025ZA, 1905035Z8, 1905035ZA, 1905065Z8, 1905105Z8, 1905135Z8, and 1905205Z8; 45-780620 - 1903045Z8, 1903115Z8, 1903135Z8, 1903135ZA, 1903155Z8, 1903185Z8, 1904055Z8, 1904085Z8, 1904105Z8, 1904155Z8, 1904225Z8, 1904245Z8, 1904265Z8, 1904295Z8, 1905025Z8, 1905035Z8, 1905065Z8, 1905085Z8, 1905105Z8, 1905105ZA, 1905135Z8, and 1905205Z8; 45-780724 - 1903045Z8, 1903185Z8, 1904085Z8, 1904105Z8, 1904265Z8, 1904295Z8, 1905025Z8, 1905035Z8, 1905085Z8, and 1905135Z8; 45-780828 - 1903045Z8, 1903065Z8, 1903085Z8, 1903115Z8, 1903135Z8, 1903155Z8, 1903205Z8, 1903225Z8, 1904055Z8, 1904085Z8, 1904155Z8, 1904265Z8, 1904295Z8, 1905035Z8, 1905155Z8, and 1905155ZA; 45-780928 - 1903045Z8, 1903115Z8, 1904055Z8, 1904155Z8, and 1904295Z8; MV-AX80202CL - 1903015Y8 and 1904015Y8; MV-AX80204CL - 1903015Y8, 1903225Y8, 1904015Y8, and 1904035Y8; MV-AX80304CL - 1903205Y8, 1903225Y8, 1904055Y8, 1905035Y8, 1905065Y8, 1905065YA, 1905135Y8, 1905155Y8, 1905175Y8, and 1905205Y8; MV-AX80308CL - 1904015Y8, 1904035Y8, 1904055Y8, 1905065Y8, 1905085Y8, 1905135Y8, 1905155Y8, 1905205Y8, and 1905225Y8; MV-AX80413CL - 1903225Y8, 1904015Y8, 1904035Y8, 1905155Y8, 1905175Y8, and 1905205Y8; MV-AX80516CL - 1903015Y8, 1903225Y8, 1904015Y8, 1904035Y8, 1905175Y8, and 1905205Y8; MV-AX80620CL - 1903045Y8, 1903225Y8, 1904015Y8, 1905065Y8, 1905085Y8, 1905155Y8, 1905175Y8, and 1905205Y8; MV-AX80724CL - 1904015Y8, 1905155Y8, 1905175Y8, and 1905205Y8; MV-AX80828CL - 1903225Y8, 1904055Y8, 1905035YA, 1905065Y8, 1905085Y8, 1905155Y8, and 1905175Y8; MV-AX80928CL - 1904035Y8 and 1905065Y8; MV-AX81032CL - 1903015Y8, 1903045Y8, 1903225Y8, 1904015Y8, 1904055Y8, 1905035YA, 1905065Y8, 1905175Y8, and 1905205Y8; MV-AX81238CL - 1904015Y8, 1904035Y8, 1905035YA, and 1905175Y8; MV-AX81434CL - 1903045Y8, 1904015Y8, 1904035Y8, and 1905065Y8; MV-AX81639CL - 1903205Y8 and 1903225Y8; and MV-AX82040CL - 1905035YA, 1905065Y8, and 1905155Y8.

Distribution pattern

The devices were distributed to Maryland. There was no direct military/government distribution. Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico.

device · product 4 of 6

Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System, REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, and MV-AZ52030HD, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.

Z-1223-2020

Recall number: Z-1223-2020
Initiated: November 24, 2019
Classification: Class II
Status: Terminated
Recalling firm: Microvention, Inc.
Quantity: 392 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The devices may be missing the implant coil.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The devices may be missing the implant coil.

Code information

Catalog/lot numbers: 45-451015 - 190410589; 45-451020- 19030456J, 19041056C, 19041756Y, 190422549, and 190422573; 45-451215 -190410569; 45-451220 -19040853N; 45-451230 -19041554R; 45-451520 -19030654N, 190408565, 190410588, and 190422572; 45-451530 -19030456L, 190408569, 19041056A, 190415571, 19041756Z, 190417599, 19042656G, and 19050254X; 45-452020 -19030456N, 19030654L, 19030655W, 19040856A, and 19041552H; 45-452030 - 19041058A, 19041554U, and 19042656H; 45-450410 - 19030456C, 19030655V, 19041058F, and 190422575; 45-450415 - 190422574; 45-450405 - 19030453C, 19030456B, and 19042254B; 45-450610 - 19030456E, 19030654W, 190410568, and 19041058E; 45-450615 - 19030456F, 190401568, 19041058C, and 19041556Y; 45-450620 - 19030453J and 19030655N; 45-450815 - 19030456G, 19030654U, 19050253U, and 19050254Z; 45-450820 - 19030453K,19030456H, 19030654R, 19030655G, 19030655H, 19050253V, 19050254Y, 19050657T, and 19051058C; and MV-AZ52030HD - 190405564.

Distribution pattern

The devices were distributed to Maryland. There was no direct military/government distribution. Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico.

device · product 5 of 6

Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers 45-651026 and 45-652050, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.

Z-1224-2020

Recall number: Z-1224-2020
Initiated: November 24, 2019
Classification: Class II
Status: Terminated
Recalling firm: Microvention, Inc.
Quantity: 19 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The devices may be missing the implant coil.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The devices may be missing the implant coil.

Code information

Catalog/lot numbers: 45-651026 - 19030655Y, 19041556W, and 19051058A; and 45-652050 - 19030654Y and 19041556X.

Distribution pattern

The devices were distributed to Maryland. There was no direct military/government distribution. Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico.

device · product 6 of 6

Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-751324, 45-751632, 45-752039, 45-750407, 45-750511, 45-750617, 45-750609, 45-750812, 45-750824, MV-AX50407CD, MV-AX50511CD, MV-AX50617CD, MV-AX50824CD, and MV-AX51019CD, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.

Z-1225-2020

Recall number: Z-1225-2020
Initiated: November 24, 2019
Classification: Class II
Status: Terminated
Recalling firm: Microvention, Inc.
Quantity: 1,187 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The devices may be missing the implant coil.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The devices may be missing the implant coil.

Code information

Catalog/lot numbers: 45-751019 - 1903045J2, 1903065J2, 1903085J2, 1904155J2, 1904175J2, 1904265J2, 1904295J2, 1905035J2, 1905085J2, 1905105K2, and 1905135J2; 45-751324 - 1903045J2, 1903155J2, 1903205J2, 1903225J2, 1904155J2, 1904225J2, 1904265J2, 1904295J2, 1905065J2, and 1905085J2; 45-751632 - 1903045J2, 1903065J2, 1903205J2, 1903225J2, 1904175J2, 1904265J2, 1904295J2, 1905035J2, 1905065J2, and 1905085J2; 45-752039 - 1903045J2, 1903205J2, 1904265J2, 1905035J2, and 1905065J2; 45-750407 - 1903045J2, 1903065J2, 1903085J2, 1903115J2, 1903155J2, 1904175J2, 1904175K2, 1904225J2, 1904245J2, 1904265J2, and1904295J2 45-750511 - 1903045J2, 1903065J2, 1903085J2, 1903155J2, 1904175J2, 1904175K2, 1904225J2, 1904245J2, 1904265J2, 1904295J2; 45-750617 - 1903045J2, 1903065J2, 1903085J2, 1903155J2, 1904055J2, 1905035J2, 1905065J2, and 1905085J2; 45-750609 - 1903045J2, 1903065J2, 1903085J2, and 1904035J2; 45-750812 - 1903045J2, 1903085J2, 1905035J2, 1905065J2, and 1905085J2; 45-750824 - 1903045J2, 1903065J2, 1903155J2 ,1904055J2, 1905035J2, 1905065J2, and 1905085J2; MV-AX50407CD - 1904015J9, 1904035J9, and 1904085J9; MV-AX50511CD - 1904015J9, 1904035J9, and 1904055J9; MV-AX50617CD - 1904015J9 and 1904035J9; MV-AX50824CD - 1904015J9 and 1904035J9; and MV-AX51019CD - 1905105J9.

Distribution pattern

The devices were distributed to Maryland. There was no direct military/government distribution. Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico.