Microvention Inc. recalls
3 recalls filed under Microvention Inc.. The most recent was published August 19, 2026.
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Class II · 2 months ago
Microvention Inc. Bobby Balloon Guide Catheter REF: BOB-895-CN BOB-895-Emea recall: Due to an increase rate of balloon pinhole defects
Due to an increase rate of balloon pinhole defects.
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Class II · 5 months ago
Microvention Inc. LVIS Intraluminal Support Device, REF/Outside Diameter xTotal Length recall: Stent-assisted coiling device may due to commingling during manufacturing
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If…
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Class II · 1+ years ago
Microvention Inc. Flow Re-Direction Endoluminal Devices: Fred 27 recall: Flow diverter may have a manufacturing issue related to the tantalum length
Flow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be…
About this page
Microvention Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.