Medline recalls specific blood pressure transducers due to particulate in fluid paths. Affected units may cause inaccurate readings or device failure. Contact Medline for details.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline is recalling certain blood pressure transducers that contain particulate in their fluid path. This could lead to inaccurate readings or device failure during use.
Particulate in the fluid path can cause blockages or inaccuracies in blood pressure measurements. This may lead to incorrect readings or device malfunction during use.
Healthcare professionals using the recalled blood pressure transducers are most at risk. Patients using these devices may experience inaccurate blood pressure readings.
Check for Medline Product Number/SKU 64037107 on the device. Lot numbers include 89181, 95326, 95254, 102287, and other numbers listed in the recall notice.
Look for Medline Product Number/SKU 64037107 and the listed lot numbers on the device.
Medline has identified particulate in the fluid path of the Manifolds, which could cause inaccurate readings or device failure.
Check for Medline Product Number/SKU 64037107 and lot numbers listed in the recall notice (e.g., 89181, 95326).
The recall does not specify a remedy, so contact Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2141-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2141-2026 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.
