ev3 Inc.: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: April 30, 2014. Most recent: March 16, 2022.

Risk classification: Class I: 2 · Class II: 3

Most recent recalls

DateAgencyProduct
March 16, 2022FDAMedtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number …Z-0695-2022
January 26, 2022FDAMedtronic HawkOne Directional Atherectomy System, Catalog numbers H1-M and H1-M-INT., Mul…Z-0450-2022
October 7, 2020FDAPacific Xtreme (PTCA Balloon Dilation Catheter)Z-3055-2020
May 4, 2016FDAev3, PowerCross" 0.018" OTW PTA Dilatation Catheter, model: AB18W030200150, Sterile EO, R…Z-1552-2016
April 30, 2014FDAev3 EverCross 0.035" OTW PTA Dilatation Catheter, 6mm x 120mm x 135cm, REF: AB35W06120…Z-1489-2014

Questions about this company

How many recalls does ev3 Inc. have?
Recalert has 5 U.S. recalls on record for ev3 Inc., published between April 30, 2014 and March 16, 2022.
What was the most recent ev3 Inc. recall?
FDA recall Z-0695-2022, published March 16, 2022: Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For use in peripheral vasculature.
Which agencies have handled ev3 Inc. recalls?
ev3 Inc. appears as the recalling firm in recalls from: FDA (5).

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