Recall Record

Sunnyvale, CA, United States

EPIX THERAPEUTICS, INC recalls

1 recall recorded since 2018, most recently on 22 February 2021. 1 is listed as ongoing. Status and classification are as published by the FDA.

Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0

Ongoing Class II Medical devices

Recall started
22 February 2021
Reason
It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.
Distribution
Product was not distributed in the US. OUS: Germany, Spain, France, Belgium, United Kingdom, Slovenia, Italy, Canada
Initiated
Voluntary: Firm initiated
Recall numbers
Z-1320-2021, Z-1321-2021, Z-1322-2021, Z-1319-2021, Z-1317-2021, Z-1318-2021

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.