Recall Z-0121-2024— Medtronic Neuromodulation

Name: FDA recall Z-0121-2024
Creator: U.S. Food and Drug Administration
Published: 2023-01-20

Class II · Ongoing

Class II FDA medical device recall by Medtronic Neuromodulation, initiated 2023-01-20. FDA's recall record names no specific 510(k) clearance for this event. Product: SenSight Connector Plug, Model Number B31061.. Reason: 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..

Recalling firm: Medtronic Neuromodulation
Classification: Class II
Status: Ongoing
Initiated: 2023-01-20
Firm location: Minneapolis, MN, United States

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.