Smiths Medical recalls HemoDraw Plus Closed Blood Sampling Sets with LogiCal Pressure Monitoring System due to reported pressure shifts and incorrect readings. Affected models include MX961H182P1, MX961H212P1, MX962H1:82P1, MX962H212P1.
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Smiths Medical is recalling HemoDraw Plus Closed Blood Sampling Sets with LogiCal Pressure Monitoring System because they may show incorrect pressure readings and shifts. This could lead to unsafe blood pressure monitoring during medical procedures.
The LogiCal Pressure Monitoring System in these sets may show incorrect pressure readings and shifts. This could lead to unsafe blood pressure monitoring during medical procedures, potentially causing complications if the pressure is misinterpreted.
Healthcare professionals using these blood sampling sets for medical procedures are most at risk. Patients receiving blood draws with these sets may experience inaccurate pressure readings.
Check for model numbers: MX961H182P1, MX961H212P1, MX962H182P1, or MX962H212P1 on the product packaging or label. These sets were sold with Smiths Medical Medex HemoDraw Plus.
Look for model numbers MX961H182P1, MX961H212P1, MX962H182P1, or MX962H212P1 on the product packaging or label.
Affected models include MX961H182P1, MX961H212P1, MX962H182P1, and MX962H212P1.
The LogiCal Pressure Monitoring System may show incorrect pressure readings and shifts, which could lead to unsafe blood pressure monitoring during medical procedures.
Check the product model number to see if it's affected. If it is, contact Smiths Medical for further instructions.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0093-2022 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0093-2022 from Smiths 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.
