Medline recalls Namic Preceptor Manifold blood pressure transducers with particulate in fluid path. Affected units have specific lot numbers and product codes. Stop using immediately to prevent potential blood contamination.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline is recalling certain blood pressure transducers due to particulate matter in the fluid path. This could lead to blood contamination during use, posing a risk to patients. Affected units have specific lot numbers and product codes.
Particulate matter in the fluid path can contaminate blood during measurements. This poses a risk of infection or other complications for patients. The particulate could enter the bloodstream if the device is used improperly.
Healthcare professionals using the Namic Preceptor Manifold blood pressure transducers with the listed lot numbers and product codes are affected. Patients receiving blood pressure measurements with these devices are at risk of contamination.
Check for the product code 64039307 and lot numbers listed: 117277, 119982, 122210, 122199, 130129, 133014, 136396, 138613, 139138, 157974, 162399, 164317, 175538, 193515, 193531.
Discontinue use of the Namic Preceptor Manifold blood pressure transducers with the listed lot numbers and product codes to prevent potential blood contamination.
The presence of particulate matter in the fluid path can lead to blood contamination during use, posing a risk of infection or complications for patients.
Affected lot numbers include 117277, 119982, 122210, 122199, 130129, 133014, 136396, 138613, 139138, 157974, 162399, 164317, 175538, 193515, and 193531.
Check for the product code 64039307 and the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2142-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2142-2026 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.
