FDA recall Z-0121-2024

Medtronic Neuromodulation · Class II · device

Product

SenSight Connector Plug, Model Number B31061.

Reason for recall

Medtronic is requesting return of a small number of units of the SenSight Connector Plug, Model B31061, due to a discrepancy in the Use By Date (UBD) printed on the label.

Distribution

US Nationwide Distribution

Key facts

Status
Ongoing
Initiation date
2023-01-20
Report date
2023-10-25
Voluntary/Mandated
Voluntary: Firm initiated
Location
Minneapolis, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0121-2024