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.
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.
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.
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.
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.
Check for the model number B31061 on the SenSight Connector Plug. Affected units have a specific lot number (082U30721) and GTIN (00763000426576).
Verify the Use By Date printed on the label matches the expected date for the product.
No, this recall is for a label discrepancy that does not pose a safety risk. The issue is only about the Use By Date label being incorrect.
Check for the model number B31061 and lot number 082U30721 with GTIN 00763000426576 on the SenSight Connector Plug.
The recall does not specify a return requirement, but you should check the label date to ensure it is correct.
We’ve drafted a message you can send Medtronic Neuromodulation to request your refund or repair — edit it as you like.
Subject: Recall Z-0121-2024 — Medtronic Neuromodulation Medtronic Neuromodulation Hello, I own a Medtronic Neuromodulation that is covered by recall Z-0121-2024 from Medtronic Neuromodulation. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
