C.R. Bard Sensica Urine Output System Recall: Measurement Accuracy Issues
C.R. Bard recalls Sensica Urine Output System with catalog number SCCS1002 due to complaints about urine output measurement accuracy. Affected units include specific lot numbers listed in the recall notice.
Lower-risk recall
Complaints relating to urine output measurement accuracy.
Contact the company
What happened, in plain English
C.R. Bard is recalling Sensica Urine Output Systems that may not measure urine output accurately. This could lead to incorrect fluid management decisions for patients using the device. The recall affects specific model numbers and lot numbers. Read more at govinfonow.com/recall/60690-c-r-bard-sensica-urine-output-system-recall-measurement-accuracy.
Source Summary by GovInfoNow · govinfonow.com/recall/60690-c-r-bard-sensica-urine-output-system-recall-measurement-accuracy · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1293-2022
Cite this page
“C.R. Bard Sensica Urine Output System Recall: Measurement Accuracy Issues.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60690-c-r-bard-sensica-urine-output-system-recall-measurement-accuracy. Based on FDA recall #Z-1293-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1293-2022%22&limit=1).
Why it’s dangerous
The device has been reported to give inaccurate urine output measurements. This could lead to improper fluid management decisions for patients, but the recall does not indicate a risk of injury or serious harm.
Who’s affected
Patients using the Sensica Urine Output System for medical monitoring are likely affected. Those with the specific catalog number SCCS1002 and listed lot numbers are most at risk.
How to tell if you have this one
Check for the catalog number SCCS1002 on the device. Affected units include specific lot numbers listed in the recall notice, such as BMFURMSF03 through BMFWRMSJ72.
- Brand
C.R. Bard- Category
Medical device
What to do — step by step
Check Product Details
Look for the catalog number SCCS1002 and the specific lot numbers listed in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 48 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-1293-2022 (May 19, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1293-2022 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.