Medline recalls 13 types of NAMIC Angiographic Manifolds with potential microscopic pinholes in sterile pouches that could lead to non-sterile conditions. Affected units have specific model numbers and expiration dates.
Potential for sterile barrier breach. Microscopic pinholes within the sterile pouch could potentially lead to non-sterile conditions.
Medline is recalling 13 different models of NAMIC Angiographic Manifolds due to microscopic pinholes in the sterile pouch that could lead to non-sterile conditions. This poses a risk for infections during medical procedures.
The sterile pouches in these manifolds may have microscopic pinholes that could allow non-sterile conditions to occur. This could lead to infections during medical procedures if the manifolds are used without proper sterility.
Healthcare professionals using these manifolds for medical procedures are most at risk. Patients undergoing procedures with these manifolds could be exposed to non-sterile conditions.
Check for model numbers starting with REF 64038301, 64038303, 70037200, 70037202, 70037301, 70037303, 70038200, 70038202, 70038301, 70038303, 70039202, 70039301, or 70039303. The manifolds were sold with expiration dates between December 31, 2023, and June 30, 2024.
Identify your manifolds using the model numbers and lot numbers listed in the recall notice.
The recall is due to potential microscopic pinholes in the sterile pouch that could lead to non-sterile conditions during medical procedures.
Check for model numbers starting with REF 64038301, 64038303, 70037200, 70037202, 70037301, 70037303, 70038200, 70038202, 70038301, 70038303, 70039202, 70039301, or 70039303. The manifolds were sold with expiration dates between December 31, 2023, and June 30, 2024.
The recall notice does not specify a remedy or action for affected manifolds.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2574-2021 — Medline Medline Hello, I own a Medline that is covered by recall Z-2574-2021 from Medline. 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.
