C.R. Bard recalls intra-abdominal pressure monitoring devices with potential for inaccurate readings due to leaks or disconnects near the sampling port. Users should confirm measurements with alternative methods.
Leaks or disconnect near the sampling port of the Intra Abdominal Pressure Monitoring Device which could lead to the potential of inaccurate readings. The measurement should be confirmed with other means, such as a new IAP system of the same kind or by choosing other diagnostic means such as but not limited to alternative systems, such as open IAP measurement options or exchanging the tubing system, which does not require invasive maneuvers.
C.R. Bard is recalling intra-abdominal pressure monitoring devices that may leak or disconnect near the sampling port, causing inaccurate readings. This could lead to incorrect medical decisions if not verified with other pressure measurement methods.
The device may leak or disconnect near the sampling port, leading to inaccurate pressure readings. This could cause incorrect medical decisions if not confirmed with alternative measurement methods.
Healthcare professionals using the device for urinary pressure monitoring are most at risk. Patients receiving this monitoring may be affected if the device provides inaccurate readings.
The device has product code IAP001 with lot numbers NGDQ2943 or NGDS0622. It was used for infusing fluid into the urinary bladder through a Foley catheter sampling port.
Verify pressure readings with alternative methods like a new IAP system or other diagnostic tools.
Product code IAP001 with lot numbers NGDQ2943 and NGDS0622.
The device may leak or disconnect near the sampling port, causing inaccurate pressure readings.
Look for product code IAP001 with lot numbers NGDQ2943 or NGDS0622.
We’ve drafted a message you can send C.R. Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1219-2020 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-1219-2020 from C.R. Bard. 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.
