Z-0121-2024 Class II Ongoing
FDA device recall Z-0121-2024 was initiated by Medtronic Neuromodulation on Jan 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
- Oct 25, 2023
- Initiation Date
- Jan 20, 2023
- 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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0121-2024
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026