Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Bard Intra-abdominal Pressure Monitoring Device is composed of a Recalled by C.R. Bard Inc Due to Leaks or disconnect near the sampling port of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact C.R. Bard Inc directly.
Affected Products
The Bard Intra-abdominal Pressure Monitoring Device is composed of a tubing set used for infusing fluid into the urinary bladder through the Foley catheter sampling port. It utilizes a clamping device to occlude the urinary drainage tubing to form a fluid column through which pressure is measured.
Quantity: 1,300 total
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About C.R. Bard Inc
C.R. Bard Inc has 65 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report