Teleflex Medical recalls Pleur-Evac Adult-Ped Wet chest drainage systems due to potential sterile packaging compromise. Affected units have specific lot numbers. Consumers should check their product details.
Potential for sterile packaging to be compromised¿
Teleflex Medical is recalling Pleur-Evac Adult-Ped Wet chest drainage systems because the sterile packaging might be compromised. This could lead to infection or other complications if the device is used without proper sterility.
The sterile packaging may become compromised, which could allow contaminants to enter the device. This might lead to infection or other complications if the device is used without proper sterility.
Patients using chest drainage systems for air/fluid evacuation, particularly those with specific lot numbers listed in the recall. Healthcare providers and patients who have purchased the device are most at risk.
Check the product code A-8000I-06 on the device. Affected units have specific lot numbers listed in the recall notice, such as 74A1801125, 74A1902739, and others.
Look for the lot numbers listed in the recall notice, such as 74A1801125, 74A1902739, and others.
The product code is A-8000I-06.
Affected lot numbers include 74A1801125, 74A1902739, 74A2000267, and others as listed in the recall notice.
The recall notice does not specify a remedy.
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2749-2020 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-2749-2020 from Teleflex Medical. 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.
