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.
Complaints relating to urine output measurement accuracy.
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.
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.
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.
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.
Look for the catalog number SCCS1002 and the specific lot numbers listed in the recall notice.
The recall is due to complaints about urine output measurement accuracy, but there is no indication of injury or serious harm. The risk is low.
Check for the catalog number SCCS1002 and the specific lot numbers listed in the recall notice, such as BMFURMSF03 through BMFWRMSJ72.
The recall does not specify a remedy, so you should check the product details to see if it is affected. If affected, contact C.R. Bard for further instructions.
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-1293-2022 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-1293-2022 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.
