Every recall we track for MICROVENTION INC. — 38 in all — plus the complaints and injury reports the public filed about them.
Microvention recalls Bobby Balloon Guide Catheters with serial numbers BOB-895-CN, BOB-895-EMEA, BOB-895-EMEA-AL, BOB-895-US, and MV-BGA01095 due to increased balloon pinhole defects.
Microvention recalls specific LVIS Intraluminal Support Devices due to potential manufacturing errors that could cause vessel injury, rupture, or neurological issues. Affected units include certain sizes and production lots.
Microvention recalls specific flow re-direction endoluminal devices due to potential incomplete deployment, which could lead to long-term health issues. Affected models include FRED 27 and related references.
Microvention recalls LIFEPEARL Drug Elutable Microspheres (200/400 micrometers) due to potential inability to reach target treatment areas, requiring additional procedures. Affected units have specific reference numbers.
MicoVention Terumo recalls specific LVIS Intraluminal Support Devices due to risk of stent not being pushed out of the introducer during use, potentially causing complications.
Microvention recalls specific microcatheter models due to potential incomplete packaging seals that could compromise sterility. Affected units include lot #0000629846. Consumers should contact Microvention for details.
Microvention recalls ERIC Retrieval Devices with incorrect 5-year expiration dates (should be 3 years). Affected models include ER173020, ER174030, and ER176044. Contact for details.
Microvention recalls HydroPearl Compressible Microspheres (REF 8HP2S600) due to manufacturing defects that may affect safety. Learn if your product is affected and what to do.
Microvention recalls AZUR CX 35 Peripheral Coil System Detachable due to potential unsealed pouch packaging. Learn if you have the affected model and what to do.
Microvention recalls FRED Flow Re-Direction Endoluminal Devices made between June 1, 2020, and September 29, 2020, due to potential incorrect inner stent length causing improper function.
Microvention recalls WEB Detachment Controller (WDC-2) due to potential implant misplacement during aneurysm embolization. Affected units have specific serial numbers sold in China and Japan. Contact for remedy.
Microvention recalls Aspiration Syringe Kit REF MVSK60 shipped to US customers without proper labeling. Affected units have specific lot and UDI codes. Stop using if you have the kit.
Microvention recalls VIA Microcatheter VIA 27 REF VIA-27-154-01 due to international labeling differences that may confuse U.S. customers. This is a single lumen catheter used in medical procedures.
Microvention recalls VIA Microcatheter VIA 17 REF VIA-17-154-01 due to international labeling differences that may cause confusion with US-cleared versions.
Microvention recalls VIA Microcatheter VIA 21 REF VIA-21-154-01 due to international labeling differences that may cause confusion with US-cleared labels.
Microvention recalls specific Terumo AZUR Peripheral Coil System models due to potential missing implant coils. Affected units have REF numbers 45-651026 and 45-652050 with specific lot numbers. Contact for remedy details.
Microvention recalls AZUR CX Peripheral Coil System (detachable 18) with specific reference numbers due to risk of missing implant coil. Affected units may require replacement.
Microvention recalls Terumo AZUR Peripheral Coil System (REF 45-451015 etc.) due to possible missing implant coils. Affected patients should contact for remedy.
Microvention recalls specific AZUR Peripheral Coil System models due to potential missing implant coils. Affected units include REF numbers 45-481015 and others. Contact for remedy details.
Microvention recalls specific Terumo AZUR Peripheral Coil System models due to potential missing implant coils. Affected units may require replacement to prevent complications.
Microvention recalls AZUR CX Peripheral Coil System (detachable 35) with REF numbers 45-751019 to 45-752039 and MV-AX codes. Devices may be missing the implant coil, which could lead to complications.
Microvention recalls specific endovascular embolization coils that may be missing the implant coil. Affected units include certain model and lot numbers. Contact Microvention for details.
Microvention recalls specific endovascular coil systems due to potential missing implant coils. Affected units have REF numbers 180520HC-R-V and 181230HC-R-V. Consumers should contact Microvention for details.
Microvention recalls endovascular embolization coils that may be missing implant coils. Check product labels for REF numbers 100102HFRM-V to MV-02508HHTA. Contact Microvention for details.
Microvention recalls certain Platinum Embolization Coils that may be missing the implant coil, which could lead to improper vascular occlusion. Affected units have specific REF numbers and catalog/lot numbers listed.
Microvention recalls specific HydroFrame 10 and HydroCoil Embolic System products that may be missing the implant coil, which could lead to incomplete treatment of vascular issues.
Microvention recalls specific endovascular embolization coil systems due to potential missing implant coils. Affected units have unique reference numbers; check your device label for details.
Microvention recalls specific endovascular coil systems due to potential missing implant coils. Affected units have unique reference numbers and lot codes. Contact Microvention for details.
Microvention recalls specific endovascular embolization coils that may be missing the implant coil. Affected units include certain REF numbers and lot codes. Consumers should check their product details to determine if they are affected.
Microvention recalls specific endovascular embolization coils that may be missing the implant coil, risking incomplete treatment of vascular malformations.
Microvention recalls certain Microplex 10 Platinum Coil Systems due to possible missing implant coils. Affected units have specific reference numbers and lot codes. Consumers should check their product details.
Microvention recalls specific endovascular coil systems due to potential missing implant coils. These coils are used in vascular procedures to block blood flow to aneurysms. Affected units have unique reference numbers and lot codes.
Microvention recalls HydroFrame 18 and HydroCoil Embolic Systems due to potential missing implant coils. Affected units have specific REF numbers and lot codes. Consumers should check their product details.
Microvention recalls certain Microplex 18 coil systems due to potential missing implant coils. Affected units may not function properly during endovascular procedures.
Microvention recalls certain Microplex 10 Platinum Coil Systems for possible missing implant coils, which could lead to incomplete treatment of vascular issues.
Microvention recalls specific endovascular coil systems due to potential missing implant coils. Affected units have unique reference numbers and may require replacement to prevent complications during vascular procedures.
Microvention recalls HydroSoft 10 and HydroCoil Embolic Systems with missing implant coils. Affected units have specific Rx/REF numbers. Contact Microvention for details.
