Overview of recall records associated with Micro Therapeutics Inc., Dba Ev3 Neurovascular, including dates, categories and classifications where available.
Classification mix: Class I: 3, Class II: 1.
Embolization device delivery system may fracture at the distal section during device implantation. A weakened bond may result in unintended separation, where the distal portion of the…
Embolization device delivery system may fracture at the distal section during device implantation. A weakened bond may result in unintended separation, where the distal portion of the…
The Distal Flush Tool (DFT) accessories that were packaged in this lot number are not compatible with the TurboHawk LX-C catheter. This may result in the inability to remove excised…
There is a potential issue for all MindFrame Capture devices to partially detach or separate from the delivery wire.
This page summarizes recall records in which the official source identifies Micro Therapeutics Inc., Dba Ev3 Neurovascular as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
