Medtronic recalls specific suction tube models due to potential unsealed sterile packing. Affected units include model numbers 10050-10061 with certain lot numbers. Consumers should check their product details to determine if they are affected.
Potential for unsealed sterile packing.
Medtronic is recalling several suction tube models because they might have unsealed sterile packaging. This could lead to contamination or infection if the tubes are used without proper sterilization. Affected products include specific model numbers and lot numbers listed in the recall notice.
The suction tubes may have unsealed sterile packaging, which could lead to contamination if the tubes are not properly sterilized before use. This poses a risk of infection or improper medical procedures if the tubes are used without adequate sterility.
Medical professionals and hospitals that use these suction tubes are most likely affected. The risk is low as the hazard involves potential contamination from unsealed packaging rather than immediate harm during use.
Check for model numbers 10050, 10052, 10053, 10060, or 10061 with specific lot numbers listed in the recall notice. The products were sold with GTINs and lot numbers from 2023041269 to 202305C077.
Identify your suction tube model number and lot numbers to see if they match the recalled items listed in the notice.
The recall is due to potential unsealed sterile packaging, which could lead to contamination. However, the hazard is low risk as the tubes themselves are not defective during normal use.
Check your product details against the model numbers and lot numbers listed in the recall notice. If affected, you may need to contact Medtronic for further instructions.
Look for model numbers 10050-10061 with specific lot numbers from 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-1804-2024 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1804-2024 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.
