FDA recall Z-2493-2019

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) · Class II · device

Product

Medtronic Micra MC1VR01, REF MC1VR01 (OUS only). Cardiac pacemaker.

Reason for recall

Medtronic is updating the Micra Instructions for Use (IFU) and the Micra Implant Procedure Tip Card to include specific information on the removal of the tether to release the Micra Pacemaker from the Micra Delivery System during implant.

Distribution

Worldwide

Key facts

Status: Terminated
Initiation date: 2019-08-06
Report date: 2019-09-18
Termination date: 2023-06-26
Voluntary/Mandated: Voluntary: Firm initiated
Location: Mounds View, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2493-2019