Smiths Medical recalls LogiCal Monitoring Set (DPS564:4005361, 4022743) due to potential insufficient welds in components that could cause leaks or failure during blood pressure monitoring.
Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks and Tubing and Medex LogiCal Kits may have been manufactured with insufficient or incomplete welds. These are components for various cardiac kits including pressure monitoring devices and interventional imaging devices.
Smiths Medical is recalling specific lots of LogiCal Monitoring Sets for blood pressure monitoring and blood sampling. The recall is because some units may have insufficient or incomplete welds in critical components, which could lead to leaks or device failure during use.
Insufficient or incomplete welds in the Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks, and Tubing could cause leaks or device failure during blood pressure monitoring. This might lead to inaccurate readings or complications for patients.
Healthcare professionals using the LogiCal Monitoring Set for blood pressure monitoring and blood sampling are most at risk. Patients receiving care from these devices could be affected if the recall lots are used.
Check the lot numbers on your LogiCal Monitoring Set (DPS564898): 4005361 or 4022743. The product is sold for blood pressure monitoring and blood sampling by Smiths Medical.
Verify your LogiCal Monitoring Set's lot number is 4005361 or 4022743.
The recalled product is LogiCal Monitoring Set, Model Number DPS564898.
Lot numbers 4005361 and 4022743 are affected.
The recall record does not specify a remedy.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1470-2021 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-1470-2021 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.
