Medtronic DLP Vessel Cannula Recall: Incorrect Labeling Hazard
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.
Lower-risk recall
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.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/56182-medtronic-dlp-vessel-cannula-recall-incorrect-labeling-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/56182-medtronic-dlp-vessel-cannula-recall-incorrect-labeling-hazard · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1316-2024
Cite this page
“Medtronic DLP Vessel Cannula Recall: Incorrect Labeling Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56182-medtronic-dlp-vessel-cannula-recall-incorrect-labeling-hazard. Based on FDA recall #Z-1316-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1316-2024%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
Check for the model number REF 30000 on the cannula. Look for lot numbers 2023020890, 202305C126, or 2023020889 on the packaging or label.
- Brand
Medtronic- Category
Medical device
What to do — step by step
Check Labeling
Verify the model number and lot numbers on the cannula packaging or label.
How this recall unfolded
Recall timeline
FDA published this recall 49 days 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.
Questions people ask
Do I need to stop using this product?
No, the recall is for incorrect labeling, not a safety hazard. You can continue using it if the labeling is correct.
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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-1316-2024 (February 7, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1316-2024 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.