Z-0121-2024 Class II Ongoing
FDA device recall Z-0121-2024 was initiated by Medtronic Neuromodulation on January 20, 2023 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 65 devices.
Recall Details
- Product Type
- Devices
- Report Date
- October 25, 2023
- Initiation Date
- January 20, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 65 devices
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.
Distribution Pattern
US Nationwide Distribution
Code Information
GTIN 00763000426576, Lot Number 082U30721