Edwards recalls specific TruWave pressure monitoring kits due to potential tubing detachment from blood sampling systems. Affected kits have a unique reference number and lot code. Contact Edwards for details.
There is a potential that the pressure tubing may detach from the blood sampling system
Edwards is recalling certain TruWave pressure monitoring kits that may have tubing that can detach from the blood sampling system. This could lead to inaccurate blood pressure readings or other complications during medical procedures.
The pressure tubing in the kit may detach from the blood sampling system during use. This could cause inaccurate blood pressure readings or disrupt the medical monitoring process, potentially leading to complications if not addressed.
Healthcare professionals using the Edwards TruWave (30 cc)/VAMP Jr Kit with reference number VMP306PX are most at risk. Patients receiving this kit during medical procedures may also be affected.
Check for the reference number VMP306PX on the kit. The lot number 63438489 is also associated with this recall. This kit is sold under the Edwards brand for medical use only.
Verify the reference number VMP306PX and lot number 63438489 on the kit.
The recall is due to a potential risk that the pressure tubing may detach from the blood sampling system, which could lead to inaccurate blood pressure readings or complications during medical procedures.
Check for the reference number VMP306PX and lot number 634389 on the kit. This specific kit is sold under the Edwards brand for medical use only.
The recall record does not specify a remedy, so contact Edwards Lifesciences directly for guidance.
We’ve drafted a message you can send Edwards to request your refund or repair — edit it as you like.
Subject: Recall Z-1964-2021 — Edwards Edwards Hello, I own a Edwards that is covered by recall Z-1964-2021 from Edwards. 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.
