Every recall we track for Micro Therapeutics, Inc. — 11 in all — plus the complaints and injury reports the public filed about them.
Micro Therapeutics recalls 3.00 mm x 12 mm embolization devices due to incorrect labeling that may lead to wrong implant size being used in intracranial aneurysm treatment.
Micro Therapeutics recalls Pipeline Flex Embolization Devices with incorrect labeling that may cause improper use in intracranial aneurysm treatment.
Micro Therapeutics recalls Pipeline Vantage Embolization Devices with Shield Technology (REFs PED3-027-350-12 to PED3-027-600-50) due to potential incomplete wall apposition and braid deformation in devices ≥4mm, which may lead to thrombosis or serious events. Higher risk in women ≤45 years.
Micro Therapeutics recalls Apollo Onyx Delivery Microcatheter (AOMC) sold in US with European indications for use. This mismatch may cause incorrect medical procedures. Contact for details.
Micro Therapeutics recalls Apollo Onyx Delivery Microcatheter (AOMC) sold in US with different indications for use than European version. This may lead to improper medical use. Contact for details.
Micro Therapeutics recalls Echelon-14 Micro Catheters with wet packaging during transport. This may cause contamination. Affected units have lot # B262322 and UDI: 847536005983.
Micro Therapeutics recalls sterile Echelon-14 microcatheters (REF 145-5092150) due to potential packaging exposure during transport. Affected units may have wet substance in outer carton.
Micro Therapeutics recalls two Axium Detachable Coil System models due to incorrect size and configuration labeling, which may lead to improper use. Affected units include QC-4-12-HELIX and QC-10-30-3D with specific lot numbers.
Micro Therapeutics recalls several Pipeline Flex Embolization Devices (PED) with specific sizes and lot numbers due to potential push wire fractures in the delivery system during use. The issue presents as a fracture in the spiral cut area of the Hypotube.
Micro Therapeutics recalls EV3 Pipeline Flex Embolization Device with Flex Shield Technology (PED2-250-10 to PED2-500-35) with specific lot numbers due to potential push wire fractures in the delivery system during use.
