Smiths Medical recalls CBSS-5ML Triple Sets (Model DPSHC0092) due to reported pressure shifts and incorrect readings in LogiCal Closed Blood Sampling Systems.
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Smiths Medical is recalling its Medex CBSS-5ML Triple Sets (Model DPSHC0:092) because they have reported issues with pressure shifts and incorrect pressure readings. This could lead to inaccurate blood pressure measurements, which might affect patient safety during medical procedures.
The sets can show incorrect pressure readings and experience pressure shifts, which may lead to inaccurate blood pressure measurements. This could result in improper medical decisions if the readings are relied upon for patient care.
Patients using the Medex CBSS-5ML Triple Sets for blood pressure monitoring are affected. Healthcare providers who use these sets for clinical purposes are at higher risk due to potential inaccuracies.
Check for the model number DPSHC0092 on the product label. The product is a Medex CBSS-5ML Triple Set with a 172/15cm size.
Look for the model number DPSHC0092 on the product label to confirm if it is recalled.
The recall indicates reported issues with pressure shifts and incorrect readings, but the product may still be safe for use if the issues are not present.
The recall does not specify a remedy, so no action is required beyond checking the product label for the model number DPSHC0092.
Check the product label for the model number DPSHC0092. The product is a Medex CBSS-5ML Triple Set with a 172/15cm size.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0101-2022 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0101-2022 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.
