ICU Medical recalls Transpac IV Monitoring Kit with Safeset Reservoir. Pressure tubing separation could delay therapy or cause blood loss, air embolism, or contamination. Check product details to take action.
Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in therapy, and in rare circumstances, pressure tubing separations could lead to blood loss, air embolism, or contamination of the fluid path.
ICU Medical is recalling a Transpac IV Monitoring Kit with Safes:et Reservoir and Blood Sampling Port. Pressure tubing separation in certain units could delay therapy or cause blood loss, air embolism, or contamination of the fluid path.
The tubing can separate between the sampling port and high pressure tubing on certain lots. This separation might delay critical therapy. In rare cases, it could cause blood loss, air embolism, or contamination of the fluid path.
Healthcare professionals using the Transpac IV Monitoring Kit with Safeset Reservoir and Blood Sampling Port are most at risk. Patients receiving IV therapy with this kit could be affected if tubing separates.
Check for the product name: ICU Medical Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60" Tubing, Disposable. Look for lot numbers 3529857 or similar on the packaging.
Look for lot numbers 3529857 or similar on the packaging to confirm if your unit is affected.
The recall reports pressure tubing separation that could delay therapy or, in rare cases, cause blood loss, air embolism, or contamination of the fluid path.
Check for lot numbers 3529857 or similar on the packaging. The product name is ICU Medical Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60" Tubing, Disposable.
The recall does not specify a remedy, so check the product details to see if it's affected. Contact ICU Medical for further instructions.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1072-2019 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1072-2019 from ICU 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.
