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Open, Classified

SenSight Connector Plug, Model Number B31061.

FDA Recall Z-0121-2024 · Posted 2023-10-18

Recalling FirmMedtronic Neuromodulation
Recall StatusOpen, Classified
Product CodeMHY
Date Initiated2023-01-20
Product Quantity65 devices

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.

Firm Action

Medtronic issued a MEDICAL DEVICE REMOVAL notice to its consignees on 01/20/2023 by mail. Consignees were asked to return any affected product they may have, and to forward this notification to those who need to be aware within the organization or to any location which the devices have been transferred.

Root Cause

Labeling Change Control

Distribution Pattern

US Nationwide Distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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