Medtronic recalls DLP Vessel Cannula model REF 30000 with incorrect labeling for specific lots. This may cause confusion in medical use. Affected units include lot numbers 2023020890, 202305C126, and 2023020889.
Medtronic is writing to inform you of incorrect labeling for three manufactured lots of the DLP Vessel Cannulae for the model and lot numbers listed above.
Medtronic is recalling DLP Vessel Cannula model REF 30000 due to incorrect labeling for three specific lots. This could lead to confusion during medical procedures, potentially affecting patient safety.
Incorrect labeling could cause healthcare providers to use the wrong cannula model during procedures. This might lead to improper medical treatment or complications if the wrong product is used.
Healthcare professionals using the DLP Vessel Cannula for medical procedures are most at risk. Patients receiving care with these specific lots may also be affected.
Check for the model number REF 30000 on the cannula. Look for lot numbers 2023020890, 202305C126, or 2023020889 on the packaging or label.
Verify the model number and lot numbers on the cannula packaging or label.
The affected model is REF 30000 with lot numbers 2023020890, 202305C126, and 2023020889.
No, the recall is for incorrect labeling, not a safety hazard. You can continue using it if the labeling is correct.
Check the model number (REF 30000) and lot numbers (2023020890, 202305C126, or 2023020889) on the packaging or label.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1316-2024 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1316-2024 from Medtronic. 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.
