Lower riskMedical device recall · FDA · Published November 15, 2023
C.R. Bard Sensica Urine Output System: Incorrect Time Display When Connected to WiFi
C.R. Bard recalls Sensica Urine Output System (SCCS1002) due to incorrect time displays when connected to WiFi, causing inaccurate monitoring data. Affected units have specific serial numbers listed in the recall.
BD (C.R. Bard) has received user complaints reporting that when the device was connected to WiFi/Internet, the time displayed on the Sensica device changed during a patient monitoring session which resulted in 1) incorrect time displayed on the monitoring screen, 2) incorrect hour block timestamps on the monitoring screen, 3) incorrect hour timestamps on data screens, and 4) incorrect catheter use time.
Take action
Contact the company
📍Recalling firmC.R. Bard Inc8195 Industrial Blvd Ne · Covington, GA 30014-1497
“C.R. Bard Sensica Urine Output System: Incorrect Time Display When Connected to WiFi.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56853-c-r-bard-sensica-urine-output-system-incorrect-time-display. Based on FDA recall #Z-0554-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0554-2024%22&limit=1).
The FDA announced on November 15, 2023, that C.R. Bard Inc is recalling Sensica Urine Output Systems due to a hazard where connected devices display incorrect time and timestamps during patient monitoring. Owners should contact the company for further instructions.
According to the FDA, C.R. Bard received user complaints reporting that when the device was connected to WiFi or the Internet, the time displayed on the Sensica device changed during a patient monitoring session. This resulted in incorrect time displayed on the monitoring screen, incorrect hour block timestamps on the monitoring screen, incorrect hour timestamps on data screens, and incorrect catheter use time.
Context
GovInfoNow's records show C.R. Bard Inc has 26 other recalls on record since June 2, 2017. Other recent recalls of similar products include the C.R. Bard Pericare Wipes Recall (June 25, 2026) and the C.R. Bard Silastic Foley Catheters Recall (April 23, 2026). A BD InLay Optima Ureteral Stent Kit recall occurred on November 6, 2025.
How to tell if you have this one
Check for the catalog number SCCS1002 on the device. Affected units have specific serial numbers listed in the recall notice, including BMGPRMYS001, BMGPRMYS003, and other serial numbers provided in the recall.
Brand
C.R. Bard
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Serial Number
Look for the serial number on the device to see if it matches the list of affected serial numbers provided in the recall.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 35 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0554-2024 (November 15, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0554-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.