Smiths Medical recalls Medex CBSS-5ML Zweifach sets with model DPSHC0090 due to reported pressure shifts and incorrect pressure 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 Medex CBSS-5ML Zweifach sets with model number DPSHC0090 because they have reported pressure shifts and incorrect pressure readings. This could lead to inaccurate blood pressure measurements, which may affect patient care.
The sets can experience pressure shifts that cause incorrect pressure readings. This means blood pressure measurements might be inaccurate, potentially leading to improper medical decisions. The hazard is specific to the LogiCal Closed Blood Sampling System sets.
Patients using the Medex CBSS-5ML Zweifach set with model DPSHC0090 for blood pressure monitoring are affected. Healthcare providers and patients who rely on accurate blood pressure readings are at the highest risk.
Check for the model number DPSHC0090 on the Medex CBSS-5ML Zweifach set. The product was sold under Smiths Medical brand with all codes.
Look for the model number DPSHC0090 on the Medex CBSS-5ML Zweifach set.
Smiths Medical recalls the Medex CBSS-5ML Zweifach set with model DPSHC0090 due to reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling Systems.
Check the model number on the set; if it's DPSHC0090, contact Smiths Medical for further instructions.
The recall is for inaccurate pressure readings, not a direct risk of serious injury. The hazard level is low risk.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0099-2022 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0099-2022 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.
