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Recalls from MICROVENTION INC.

Recalls from MICROVENTION INC. filed with the FDA, USDA FSIS, CPSC or NHTSA, newest first. Company page 2 recalls Each recall is dated by the day its recall page names (how recalls are dated).
Agency
Risk level
Status
Date
Sold in

1 recall that day

BOBBY Balloon Guide Catheter

The BOBBY Balloon Guide Catheter has an increased rate of balloon pinhole defects.

Moderate risk, FDA, Device defect

1 recall that day

LVIS Intraluminal Support Device

The LVIS Intraluminal Support Device may have dimensional nonconformance or incorrect configuration, potentially causing vessel injury or neurological events.

Moderate risk, FDA, Device defect