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FDA (Device enforcement)Recalled 2022-05-19class ii

C.R. Bard Inc: Sensica Urine Output System

Is my product affected?

Sensica Urine Output System

  • UPC 0801741215773

Check against the official notice below — it lists the full affected range.

What happened

C.R. Bard Inc. is recalling the Sensica Urine Output System due to complaints about the accuracy of urine output measurements. A total of 457 units have been distributed nationwide. The affected product is Catalog Number SCCS1002, and consumers can identify recalled units by checking if their device matches any of the listed lot numbers.

The recall record does not specify what remedy is available to affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Complaints relating to urine output measurement accuracy.

Details from the source

Reason for recall: Complaints relating to urine output measurement accuracy. Distribution: US Nationwide. Quantity: 457 units Lot/code info: UDI: (01) 0 0801741215773; Catalog Number: SCCS1002 (Lot Numbers: BMFURMSF03, BMFURMSF07, BMFURMSF08, BMFURMSF10, BMFURMSF12, BMFURMSF13, BMFURMSF15, BMFURMSF16, BMFURMSF18, BMFURMSF19, BMFURMSF20, BMFURMSF22, BMFURMSF23, BMFURMSF24, BMFURMSF25, BMFURMSF26, BMFURMSF27, BMFURMSF28, BMFURMSF29, BMFURMSF30, BMFURMSF31, BMFURMSF32, BMFURMSF33, BMFURMSF34, BMFURMSF35, BMFURMSF36, BMFURMSF37, BMFURMSF38, BMFURMSF39, BMFURMSF40, BMFURMSF41, BMFURMSF42, BMFURMSF43, BMFURMSF44, BMFURMSF45, BMFURMSF46, BMFURMSF47, BMFURMSF48, BMFURMSF49, BMFURMSF50, BMFURMSF51, BMFURMSF52, BMFURMSF53, BMFURMSF54, BMFURMSF55, BMFURMSF56, BMFURMSF57, BMFURMSF58, BMFURMSF59, BMFURMSF60, BMFVRMSQ82, BMFVRMSQ84, BMFVRMSQ85, BMFVRMSQ86, BMFVRMSQ87, BMFVRMSQ88, BMFVRMSQ92, BMFVRMSQ94, BMFVRMSQ95, BMFVRMSQ96, BMFVRMSQ97, BMFVRMSQ98, BMFVRMSQ99, BMFVRMSR00, BMFVRMSR01, BMFVRMSR02, BMFVRMSR05, BMFVRMSR06, BMFVRMSR07, BMFVRMSR08, BMFVRMSR09, BMFVRMSR10, BMFVRMSR11, BMFVRMSR12, BMFVRMSR13, BMFVRMSR14, BMFVRMSR15, BMFVRMSR19, BMFVRMSR20, BMFVRMSR22, BMFVRMSR23, BMFVRMSR24, BMFVRMSR25, BMFVRMSR26, BMFVRMSR27, BMFVRMSR28, BMFVRMSR29, BMFVRMSR31, BMFVRMSR34, BMFVRMSR36, BMFVRMSR37, BMFVRMSR38, BMFVRMSR39, BMFVRMSR40, BMFWRMSBR6, BMFWRMSBR7, BMFWRMSBR8, BMFWRMSBR9, BMFWRMSBS0, BMFWRMSBS1, BMFWRMSBS2, BMFWRMSBS3, BMFWRMSBS4, BMFWRMSBS5, BMFWRMSBS6, BMFWRMSBS7, BMFWRMSBS8, BMFWRMSBS9, BMFWRMSBT0, BMFWRMSBT1, BMFWRMSBT2, BMFWRMSBT3, BMFWRMSBT4, BMFWRMSBT5, BMFWRMSBT6, BMFWRMSBT7, BMFWRMSBT8, BMFWRMSBT9, BMFWRMSBU0, BMFWRM

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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