Smiths Medical recalls Mark 910 LogiCal blood pressure monitoring devices with insufficient welds in specific lots. Affected units may cause leaks or failures during use. Contact for return instructions.
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 Mark 910 LogiCal blood pressure monitoring devices due to potential insufficient or incomplete welds in components. This could lead to leaks or failures during use, posing a risk of inaccurate readings or device malfunction.
Insufficient or incomplete welds in the Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks, and Tubing could cause leaks or failures during use. This might lead to inaccurate blood pressure readings or device malfunction, potentially affecting medical treatment.
Patients using blood pressure monitoring devices or blood sampling equipment with the specific lot numbers listed. Healthcare providers and individuals with medical devices that use these components are most at risk.
Check for the model number DPS567201 on the device. Affected units have lot number 4031331. This recall applies to specific lots manufactured for blood pressure monitoring and blood sampling devices.
Look for the lot number 4031331 on the device to confirm if it is affected.
The model number is DPS567201 for blood pressure monitoring and blood sampling devices.
Check for lot number 4031331 on the device.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1471-2021 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-1471-2021 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.
