Medtronic recalls Clearview Blower/Mister model 22120 (lot 2023040203, 2023040473) due to potential unsealed sterile packing. Affected units may pose infection risks during medical procedures.
Potential for unsealed sterile packing.
Medtronic is recalling its Clearview Blower/Mister model 22120 because the sterile packaging might not seal properly. This could lead to infection risks during medical procedures if the device is used without proper sterilization.
The sterile packaging may become unsealed during shipping or storage, allowing contaminants to enter the device. This could lead to infections if the device is used without proper sterilization during medical procedures.
Patients using this medical device for procedures like surgery or therapy. Healthcare providers who handle the device are most at risk of infection exposure.
Check for model number 22120 on the device. Units sold with lot numbers 2023040203 or 2023040473 are affected.
Look for model number 22120 and lot numbers 2023040203 or 2023040473 on the device packaging.
The recall indicates a potential risk of unsealed sterile packaging, which could lead to infection if not properly sterilized. The device may still be safe if handled correctly, but the recall advises checking for affected units.
Check for model number 22120 and lot numbers 2023040203 or 2023040473 on the device packaging.
The recall does not specify a remedy, so contact Medtronic directly for guidance on whether to use or discard the device.
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-1794-2024 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1794-2024 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.
