Manufacturer

Microvention, Inc.

38 recalls in our database name Microvention, Inc. as the manufacturing or recalling firm.

What the numbers show

Total: 38
Critical: 0
Severe: 3
Most recent: 2026-08-19

Of the 38 recalls from Microvention, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (8%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

26–38 of 38

HighFDA (Devices)·Z-1398-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 3,442 units of Platinum Coil Systems because the implant coil may be missing from the packaging.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Cosmos 10, Sterile, Rx, REF numbers 100202CSSR-V, 100254CSSR-V, 100306CSSR-V, 100408CSSR-V, 100412CSSR-V, 100515CSSR-V, 100522CSSR-V, 100618CSSR-V, 100626CSSR-V, 100722CSSR-V, 100731CSSR-V,
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1407-2020·2020-03-04
MicroVention Platinum Coil System Recall for Missing Implant Coils
MicroVention is recalling Microplex 10 Platinum Coil Systems because the implant coil may be missing from the packaging.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft Helical, Sterile, Rx, REF numbers 100101HS-V, 100102HS-V, 100103HS-V, 100104HS-V, 100151HS-V, 100152HS-V, 100153HS-V, 100154HS-V, 100201HS-V, 100202HS-V, 100203HS-V, 100204HS-V, 100
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1401-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 19 units of the Microplex 18 Platinum Coil System because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil, Complex 18, Sterile, Rx, REF numbers 180512CC-V, 180820CC-V, 181026CC-V, 181434CC-V, and 182050CC-V. Product Usage: The MCS is also intended for vascular occlusion of blood vessels within t
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1400-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling Microplex 10 Platinum Coil Systems because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Complex 10, Sterile, Rx, REF numbers 100204CC-V, 100307CC-V, 100410CC-V, 100512CC-V, 100615CC-V, 100718CC-V, 100820CC-V, 100924CC-V, and 101026CC-V. Product Usage: The MCS is also intended
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1405-2020·2020-03-04
MicroVention HydroSoft Embolization Coils Recalled for Missing Implant Coils
MicroVention is recalling 847 HydroSoft embolization coils because the implant coil may be missing from the packaging. The devices were distributed to 43 countries outside the United States.
Product
MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, HydroSoft 3D, Sterile, Rx, REF numbers 100102HFRM-V, 100152HFRM-V, 100153HFRM-V, 100154HFRM-V, 100202HFRM-V, 100206HFRM-V, 100208HFRM-V, 100254HFRM-V, 100256HFRM-V, 100308HFRM-V, MV-00202
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1396-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 9 units of Microplex 18 Platinum Coil Systems because the implant coil may be missing from the packaging.
Product
MicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil, Helical 18 Regular, Sterile, Rx, REF numbers 180520HC-R-V and 181230HC-R-V. Product Usage: The MCS is also intended for vascular occlusion of blood vessels within the neurovascular system
Category
Medical Device
Distribution
1 state
SevereFDA (Devices)·Z-1223-2020·2020-02-19
Microvention AZUR Peripheral Coil System Recall for Missing Implant Coil
Microvention is recalling 392 units of AZUR Peripheral Coil Systems because the implant coil may be missing from the devices.
Product
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, 4
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1220-2020·2020-02-19
Terumo AZUR Peripheral Coil System Recalled for Missing Implant Coil
Microvention, Inc. is recalling 445 units of Terumo AZUR Peripheral Coil Systems because the implant coil may be missing from the device.
Product
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
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1221-2020·2020-02-19
MicroVention AZUR Peripheral Coil System Recalled for Missing Implant Coil
MicroVention is recalling 107 units of the AZUR Peripheral Coil System because the implant coil may be missing from the sterile packaging.
Product
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.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1225-2020·2020-02-19
Terumo AZUR CX Peripheral Coil System Recalled for Missing Implant Coil
Microvention is recalling 1,187 units of Terumo AZUR CX Peripheral Coil Systems because the implant coil may be missing from the packaging.
Product
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 fi
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1222-2020·2020-02-19
Terumo AZUR CX Peripheral Coil System Recalled for Missing Implant Coil
Microvention, Inc. is recalling 3,881 units of the Terumo AZUR CX Peripheral Coil System because the devices may be missing the implant coil.
Product
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, M
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1224-2020·2020-02-19
Terumo AZUR Peripheral Coil System Recalled for Missing Implant Coil
Microvention, Inc. is recalling 19 units of Terumo AZUR Peripheral Coil Systems because the implant coil may be missing from the device.
Product
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.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-3103-2017·2017-09-13
MicroVention Traxcess 7 Mini Guidewire Recalled for Coating Delamination
MicroVention is recalling 34 units of Traxcess 7 Mini Guidewires because the hydrophilic coating may delaminate from the device.
Product
MicroVention Terumo Traxcess 7 Mini Guidewire with Hydrophilic Coating, Ref GW0721006M, 1 guidewire per package, sterile, RX.
Category
Medical Device
Distribution
12 states