C.R. Bard, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0488-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

BARD UROS AUTOMATED URINE OUPTUT AND TEMPERATURE MONITOR, MODEL BK10001M The Uros(TM) Automated Urine Output and Temperature Monitor is indicated to monitor urine output and core bladder temperature.

Product Classification:

Class II

Date Initiated: September 29, 2017

Date Posted: February 7, 2018

Recall Number: Z-0488-2018

Event ID: 78231

Reason for Recall:

The possibility exists that use of the Uros Automated Urine Output and Temperature Monitor may lead to the loss of urine output measurement data and/or urine output measurement inaccuracies resulting in an impact on clinical treatment decisions.

Status: Terminated

Product Quantity: 2 units

Code Information:

Catalog/PC #BK10001M

Distribution Pattern:

US Distribution to the state of: FL

Voluntary or Mandated:

Voluntary: Firm initiated