Smiths Medical recalls LogiCal 5mL Closed Blood Sampling Systems with specific model numbers due to reported pressure shifts and incorrect pressure readings.
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Smiths Medical is recalling certain LogiCal 5mL Closed Blood Sampling Systems because they may cause incorrect pressure readings. This could lead to improper medical decisions if used in blood sampling procedures.
The recalled blood sampling systems may show incorrect pressure readings due to pressure shifts. This could lead to improper medical decisions if the readings are used for critical patient monitoring.
Healthcare professionals using the recalled models for blood sampling are most at risk. Patients receiving blood samples from these systems could be affected if the pressure readings are inaccurate.
Check the model number on the packaging or label. The affected models include MX961E181P1, MX961E211P1, MX962E211P1, MX96AE181P1, and MX96AE211P1.
Look for the model number on the packaging or label to confirm if your system is affected.
Smiths Medical reports that the LogiCal 5mL Closed Blood Sampling Systems may cause incorrect pressure readings due to pressure shifts.
The affected models are MX961E181P1, MX961E211P1, MX962E211P1, MX96AE181P1, and MX96AE211P1.
No action is required beyond checking the model number. The recall does not require immediate discontinuation.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0092-2022 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0092-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
