FDA Device recall Z-2243-2018
CritiCore Automated Urine Output and Temperature Monitor
- FDA Device
- Class II
- ongoing
- Published 2018-06-27
On 2018-06-27 the FDA classified a Class II recall of CritiCore Automated Urine Output and Temperature Monitor by C R Bard, citing issues identified with the monitor including urine output measurement errors, temperature measurement errors and undesired alarms.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2243-2018 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-11-10 |
| Published | 2018-06-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | C R Bard |
| Distribution | AR, AZ, CA, FL, GA, HI, IN, KS, LA, MD, MN, MO, MS, NC, NJ, OH, OK, TN, TX, VA, WA, WI, WY |
Product
CritiCore Automated Urine Output and Temperature Monitor
Reason
Issues identified with the monitor including urine output measurement errors, temperature measurement errors and undesired alarms.
Identifiers
| code_info | DYZIAA003, DYAPAA017, DYARAA002, DYARAA047, DYBPAA012, DYBRAA022, DYBSAA022, DYBSAA067, DYZIAA004, DYAPAA018, DYARAA003…DYZIAA003, DYAPAA017, DYARAA002, DYARAA047, DYBPAA012, DYBRAA022, DYBSAA022, DYBSAA067, DYZIAA004, DYAPAA018, DYARAA003, DYARAA048, DYBPAA013, DYBRAA023, DYBSAA023, DYBSAA068, DYZIAA005, DYAPAA019, DYARAA004, DYARAA049, DYBPAA014, DYBRAA024, DYBSAA024, DYBSAA069, DYZIAA006, DYAPAA020, DYARAA005, DYARAA050, DYBPAA015, DYBRAA025, DYBSAA025, DYBSAA070, DYZIAA007, DYAQAA001, DYARAA006, DYARAA051, DYBPAA016, DYBRAA026, DYBSAA026, DYBSAA071, DYZIAA008, DYAQAA002, DYARAA007, DYARAA052, DYBPAA017, DYBRAA027, DYBSAA027, DYBSAA072, DYZIAA009, DYAQAA003, DYARAA008, DYARAA053, DYBPAA018, DYBRAA028, DYBSAA028, DYBSAA073, DYZIAA010, DYAQAA004, DYARAA009, DYARAA054, DYBPAA019, DYBRAA029, DYBSAA029, DYBSAA074, DYZJAA001, DYAQAA005, DYARAA010, DYARAA055, DYBPAA020, DYBRAA030, DYBSAA030, DYBSAA075, DYZKAA001, DYAQAA006, DYARAA011, DYARAA056, DYBQAA001, DYBRAA031, DYBSAA031, DYBSAA076, DYZKAA002, DYAQAA007, DYARAA012, DYARAA057, DYBQAA002, DYBRAA032, DYBSAA032, DYBSAA077, DYZKAA003, DY |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2243-2018%22
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