Microvention, Inc.: 15 recalls on record

Recalls filed with 1 agency: FDA (15).

First recall on record: September 13, 2017. Most recent: August 19, 2026.

Risk classification: Class II: 15

Most recent recalls

DateAgencyProduct
August 19, 2026FDABOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US…Z-2912-2026
May 20, 2026FDALVIS Intraluminal Support Device, REF/Outside Diameter(OD)xTotal Length(TL)xWorking Lengt…Z-2200-2026
January 29, 2025FDAMicrovention, Headway" 17 Advanced Straight Microcatheter with Hydrophilic Coating, REF: …Z-0990-2025
September 25, 2024FDAERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is…Z-3157-2024
February 7, 2024FDATERUMO HydroPearl Compressible Microspheres for Embolisation REF 8HP2S600Z-0868-2024
March 4, 2020FDAMicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, C…Z-1404-2020
March 4, 2020FDAMicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, H…Z-1395-2020
March 4, 2020FDAMicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coi…Z-1392-2020
March 4, 2020FDAMicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil, H…Z-1397-2020
March 4, 2020FDAMicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, H…Z-1407-2020
March 4, 2020FDAMicroVention Terumo HydroFrame 18, HydroCoil Embolic System, Endovascular Embolization Co…Z-1403-2020
March 4, 2020FDAMicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil, C…Z-1401-2020
February 19, 2020FDATerumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-…Z-1225-2020
February 19, 2020FDATerumo AZUR Peripheral Coil System, Detachable 18, Framing Coil, REF numbers 45-681026, 4…Z-1221-2020
September 13, 2017FDAMicroVention Terumo Traxcess 7 Mini Guidewire with Hydrophilic Coating, Ref GW0721006M, 1…Z-3103-2017

Questions about this company

How many recalls does Microvention, Inc. have?
Recalert has 15 U.S. recalls on record for Microvention, Inc., published between September 13, 2017 and August 19, 2026.
What was the most recent Microvention, Inc. recall?
FDA recall Z-2912-2026, published August 19, 2026: BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an intravascular catheter into a select…
Which agencies have handled Microvention, Inc. recalls?
Microvention, Inc. appears as the recalling firm in recalls from: FDA (15).

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