It has been determined that product manufactured between June 1, 2020, and September 29, 2020, may be manufactured with an incorrect inner stent length and may not perform as intended. Recall start date: June 7, 2023
Hazard description
Performance
Product
Product name
Fred® Flow Re-Direction Endoluminal Device
Reference
ID
RA-74058
Get notified of similar recallsEnter your email to receive alerts when new recalls are issued by the same agency.
Subscribed. You'll get an email when new recalls are issued.
RecallTracker