Recall Z-2623-2014— Medtronic Cardiovascular Surgery-the Heart Valve Division
Class II · Terminated
Class II FDA medical device recall by Medtronic Cardiovascular Surgery-the Heart Valve Division, initiated 2014-08-15, terminated 2014-11-06. FDA's recall record names no specific 510(k) clearance for this event. Product: Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012. Used use in conjunction with Hancock Conduit Model 105 to provide an alternate method for relief of left ventricular hypertension.. Reason: Medtronic has decided to discontinue production and distribution of this low-volume product..
- Recalling firm
- Medtronic Cardiovascular Surgery-the Heart Valve Division
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-08-15
- Terminated
- 2014-11-06
- Firm location
- Santa Ana, CA, United States
Product description
Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012. Used use in conjunction with Hancock Conduit Model 105 to provide an alternate method for relief of left ventricular hypertension.
Reason for recall
Medtronic has decided to discontinue production and distribution of this low-volume product.
Data sourced from openFDA. This site is unofficial and independent of the FDA.