Medtronic recalls specific venous cannula models due to potential unsealed sterile packing. Affected units include various sizes and model numbers with specific lot numbers. Consumers should check their product details and contact Medtronic for guidance.
Potential for unsealed sterile packing.
Medtronic is recalling several venous cannula models that may have unsealed sterile packing. This could lead to contamination or infection if used improperly. Affected products include specific sizes and model numbers with listed lot numbers.
The venous cannulae may have unsealed sterile packaging, which could lead to contamination or infection if the product is used without proper sterilization. This is a risk during medical procedures where sterile conditions are critical.
Healthcare professionals and patients using the recalled venous cannulae for medical procedures are most at risk. The recall affects specific model numbers and lot numbers listed in the notice.
Check the model number and lot number on the product. Affected models include sizes from 12 to 36 French with specific model numbers like 68120, 68124, and others listed in the recall notice. Lot numbers are also specified for each model.
Identify the model number and lot number on the cannula to see if it matches the affected list provided in the recall.
The recall includes specific venous cannula models with sizes from 12 to 36 French, such as model numbers 68120, 68124, 68128, and others listed in the notice with corresponding lot numbers.
Check the model number and lot number on the product. Affected products are listed in the recall notice with specific model numbers and lot numbers.
The recall does not specify a remedy, so contact Medtronic directly for guidance on next steps.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1805-2024 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1805-2024 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.
