Medtronic recalls DLP 1 mm Arteriotomy Cannula model 31001 with unsealed sterile packing. Affected units include specific lot numbers and GTINs sold in 2023. Consumers should check their product details and contact Medtronic for guidance.
Potential for unsealed sterile packing.
Medtronic is recalling DLP 1 mm Arteriotomy Cannulae model 31001 due to potential unsealed sterile packing. This could lead to contamination or infection if the cannula is used without proper sterilization. Affected units have specific lot numbers and GTINs listed in the recall.
The sterile packing may not be sealed properly, leading to contamination. If the cannula is used without proper sterilization, it could cause infections or other complications during medical procedures.
Medical professionals using the cannula for procedures may be affected. Patients receiving the cannula during surgery are at risk if the sterile packing is compromised.
Check for the model number 31001 on the product. Look for specific lot numbers: 2023041316, 2023041318, 2023041320, 2023041323, 202305C146, 202305C154. The product also has GTINs: 00613994575319, 00673978180465, 20613994575313.
Identify the model number (31001) and lot numbers listed in the recall notice.
The recalled model number is 31001.
Affected lot numbers include 2023041316, 2023041318, 2023041320, 2023041323, 202305C146, and 202305C154.
Check the model number (31001) and lot numbers on your product against the list provided in the recall notice.
We’ve drafted a message you can send Medtronic Perfusion Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1796-2024 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1796-2024 from Medtronic Perfusion Systems. 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.
