Medtronic SenSight Connector Plug Recall: Use By Date Label Discrepancy
Medtronic is recalling a small number of SenSight Connector Plug Model B31061 units due to a discrepancy in the Use By Date label. Affected units have a specific lot number and GTIN.
Lower-risk 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.
Contact the company
What happened, in plain English
Medtronic is recalling a small number of SenSight Connector Plug units (Model B31061) because the Use By Date printed on the label is incorrect. This discrepancy could lead to confusion about when the product should be used, but it does not pose a safety risk. Read more at govinfonow.com/recall/59022-medtronic-sensight-connector-plug-recall-use-by-date-label-discrepancy.
Source Summary by GovInfoNow · govinfonow.com/recall/59022-medtronic-sensight-connector-plug-recall-use-by-date-label-discrepancy · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0121-2024
Cite this page
“Medtronic SenSight Connector Plug Recall: Use By Date Label Discrepancy.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59022-medtronic-sensight-connector-plug-recall-use-by-date-label-discrepancy. Based on FDA recall #Z-0121-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0121-2024%22&limit=1).
Why it’s dangerous
The Use By Date label on the SenSight Connector Plug has an incorrect date, which could cause users to misunderstand when the product is safe to use. This discrepancy does not involve physical hazards like injury or malfunction but may lead to confusion about the product's validity.
Who’s affected
Users of the SenSight Connector Plug Model B31061 with the specific lot number 082U30721 and GTIN 00763000426576 are affected. Patients using this device for medical purposes may be at risk of confusion about the product's expiration date.
How to tell if you have this one
Check for the model number B31061 on the SenSight Connector Plug. Affected units have a specific lot number (082U30721) and GTIN (00763000426576).
- Brand
Medtronic Neuromodulation- Product
SenSight Connector Plug, Model Number B31061- Category
Medical device
What to do — step by step
Check Label Date
Verify the Use By Date printed on the label matches the expected date for the product.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide Distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0121-2024 (January 20, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0121-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.