PlainRecalls
FDA Devices Moderate Class II Ongoing

CritiCore Automated Urine Output and Temperature Monitor

Reported: June 27, 2018 Initiated: November 10, 2017 #Z-2243-2018

Product Description

CritiCore Automated Urine Output and Temperature Monitor

Reason for Recall

Issues identified with the monitor including urine output measurement errors, temperature measurement errors and undesired alarms.

Details

Recalling Firm
C.R. Bard, Inc.
Units Affected
N/A
Distribution
AR, AZ, CA, FL, GA, HI, IN, JP, KS, LA, MD, MN, MO, MS, NC, NJ, OH, OK, TN, TX, VA, WA, WI, and WY
Location
Covington, GA

Frequently Asked Questions

What product was recalled?
CritiCore Automated Urine Output and Temperature Monitor. Recalled by C.R. Bard, Inc.. Units affected: N/A.
Why was this product recalled?
Issues identified with the monitor including urine output measurement errors, temperature measurement errors and undesired alarms.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 27, 2018. Severity: Moderate. Recall number: Z-2243-2018.