Medtronic Perfusion Systems recalls Medtronic DLP Vessel Cannula, Model Number REF 30000
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.
Read the official notice →- Date
- 2024-03-27
- Country
- United States
- Brand
- Medtronic Perfusion Systems
- Product
- Medtronic DLP Vessel Cannula, Model Number REF 30000
- Classification
- Class II
- Units
- US and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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