SenSight Connector Plug, Model Number B31061.
FDA device recall Z-0121-2024 · posted 2023-10-18 · Open, Classified
Recall details
- Recalling firm
- Medtronic Neuromodulation
- 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.
- Action taken
- 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
- Status
- Open, Classified
- Product code
- MHY
- Quantity affected
- 65 devices
- Distribution
- US Nationwide Distribution
- Date initiated
- 2023-01-20
- Date posted
- 2023-10-18
- Location
- Minneapolis, MN
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