—#164531

Product

CritiCore Automated Urine Output and Temperature Monitor

FDA product code: EXS — Urinometer, Electrical
Device class: Class 2
Medical specialty: Gastroenterology, Urology
Affected lot / code info: 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, DYAQAA008, DYARAA013, DYARAA058, DYBQAA003, DYBRAA033, DYBSAA033, DYBSAA078, DYZKAA004, DYAQAA009, DYARAA014, DYARAA059, DYBQAA004, DYBRAA034, DYBSAA034, DYBSAA079, DYZKAA005, DYAQAA010, DYARAA015, DYARAA060, DYBQAA005, DYBRAA035, DYBSAA035, DYBSAA080, DYZKAA006, DYAQAA011, DYARAA016, DYASAA001, DYBQAA006, DYBRAA036, DYBSAA036, DYBSAA081, DYZKAA007, DYAQAA012, DYARAA017, DYASAA002, DYBQAA007, DYBRAA037, DYBSAA037, DYBSAA082, DYZKAA008, DYAQAA013, DYARAA018, DYASAA003, DYBQAA008, DYBRAA038, DYBSAA038, DYBSAA083, DYZKAA009, DYAQAA014, DYARAA019, DYASAA004, DYBQAA009, DYBRAA039, DYBSAA039, DYBSAA084, DYZKAA010, DYAQAA015, DYARAA020, DYASAA005, DYBQAA010, DYBRAA040, DYBSAA040, DYBSAA085, DYZKAA011, DYAQAA016, DYARAA021, DYASAA006, DYBQAA011, DYBRAA041, DYBSAA041, DYBSAA086, DYZKAA012, DYAQAA017, DYARAA022, DYASAA007, DYBQAA012, DYBRAA042, DYBSAA042, DYBSAA087, DYZKAA013, DYAQAA018, DYARAA023, DYASAA008, DYBQAA013, DYBRAA043, DYBSAA043, DYBSAA088, DYZKAA014, DYAQAA019, DYARAA024, DYASAA009, DYBQAA014, DYBRAA044, DYBSAA044, DYBSAA089, DYZKAA015, DYAQAA020, DYARAA025, DYASAA010, DYBQAA015, DYBRAA045, DYBSAA045, DYBSAA090, DYZKAA016, DYAQAA021, DYARAA026, DYASAA011, DYBRAA001, DYBSAA001, DYBSAA046, DYBSAA091, DYZKAA017, DYAQAA022, DYARAA027, DYASAA012, DYBRAA002, DYBSAA002, DYBSAA047, DYBSAA092, DYZKAA018, DYAQAA023, DYARAA028, DYASAA013, DYBRAA003, DYBSAA003, DYBSAA048, DYBSAA093, DYZKAA019, DYAQAA024, DYARAA029, DYASAA014, DYBRAA004, DYBSAA004, DYBSAA049, DYBSAA094, DYZKAA020, DYAQAA025, DYARAA030, DYASAA015, DYBRAA005, DYBSAA005, DYBSAA050, DYBSAA095, DYAPAA001, DYAQAA026, DYARAA031, DYASAA016, DYBRAA006, DYBSAA006, DYBSAA051, DYBSAA096, DYAPAA002, DYAQAA027, DYARAA032, DYASAA017, DYBRAA007, DYBSAA007, DYBSAA052, DYBSAA097, DYAPAA003, DYAQAA028, DYARAA033, DYASAA018, DYBRAA008, DYBSAA008, DYBSAA053, DYBSAA098, DYAPAA004, DYAQAA029, DYARAA034, DYASAA019, DYBRAA009, DYBSAA009, DYBSAA054, DYBSAA099, DYAPAA005, DYAQAA030, DYARAA035, DYASAA020, DYBRAA010, DYBSAA010, DYBSAA055, DYBSAA100, DYAPAA006, DYAQAA031, DYARAA036, DYBPAA001, DYBRAA011, DYBSAA011, DYBSAA056, DYBTAA001, DYAPAA007, DYAQAA032, DYARAA037, DYBPAA002, DYBRAA012, DYBSAA012, DYBSAA057, DYBTAA002, DYAPAA008, DYAQAA033, DYARAA038, DYBPAA003, DYBRAA013, DYBSAA013, DYBSAA058, DYBTAA003, DYAPAA009, DYAQAA034, DYARAA039, DYBPAA004, DYBRAA014, DYBSAA014, DYBSAA059, DYBTAA004, DYAPAA010, DYAQAA035, DYARAA040, DYBPAA005, DYBRAA015, DYBSAA015, DYBSAA060, DYBTAA005, DYAPAA011, DYAQAA036, DYARAA041, DYBPAA006, DYBRAA016, DYBSAA016, DYBSAA061, DYBTAA006, DYAPAA012, DYAQAA037, DYARAA042,DYBPAA007, DYBRAA017, DYBSAA017, DYBSAA062, DYBTAA007, DYAPAA013, DYAQAA038, DYARAA043, DYBPAA008, DYBRAA018, DYBSAA018, DYBSAA063, DYBTAA008, DYAPAA014, DYAQAA039, DYARAA044, DYBPAA009, DYBRAA019, DYBSAA019, DYBSAA064, DYBTAA009, DYBTAA010, DYBTAA027, DYBTAA044, DYBUAA001, DYBUAA018, DYBUAA035, DYBUAA052, DYBUAA069, DYBTAA011, DYBTAA028, DYBTAA045, DYBUAA002, DYBUAA019, DYBUAA036, DYBUAA053, DYBUAA070, DYBTAA012, DYBTAA029, DYBTAA046, DYBUAA003, DYBUAA020, DYBUAA037, DYBUAA054, DYBUAA071, DYBTAA013, DYBTAA030, DYBTAA047, DYBUAA004, DYBUAA021, DYBUAA038, DYBUAA055, DYBUAA072, DYBTAA014, DYBTAA031, DYBTAA048, DYBUAA005, DYBUAA022, DYBUAA039, DYBUAA056, DYBUAA073, DYBTAA015, DYBTAA032, DYBTAA049, DYBUAA006, DYBUAA023, DYBUAA040, DYBUAA057, DYBUAA074, DYBTAA016, DYBTAA033, DYBTAA050, DYBUAA007, DYBUAA024, DYBUAA041, DYBUAA058, DYBUAA075, DYBTAA017, DYBTAA034, DYBTAA051, DYBUAA008, DYBUAA025, DYBUAA042, DYBUAA059, DYBUAA076, DYBTAA018, DYBTAA035, DYBTAA052, DYBUAA009, DYBUAA026, DYBUAA043, DYBUAA060, DYBUAA077, DYBTAA019, DYBTAA036, DYBTAA053, DYBUAA010, DYBUAA027, DYBUAA044, DYBUAA061, DYBUAA078, DYBTAA020, DYBTAA037, DYBTAA054, DYBUAA011, DYBUAA028, DYBUAA045, DYBUAA062, DYBUAA079, DYBTAA021, DYBTAA038, DYBTAA055, DYBUAA012, DYBUAA029, DYBUAA046, DYBUAA063, DYBUAA080, DYBTAA022, DYBTAA039, DYBTAA056, DYBUAA013, DYBUAA030, DYBUAA047, DYBUAA064, DYBTAA023, DYBTAA040, DYBTAA057, DYBUAA014, DYBUAA031, DYBUAA048, DYBUAA065, DYBTAA024, DYBTAA041, DYBTAA058, DYBUAA015, DYBUAA032, DYBUAA049, DYBUAA066, DYBTAA025, DYBTAA042, DYBTAA059, DYBUAA016, DYBUAA033, DYBUAA050, DYBUAA067, DYBTAA026, DYBTAA043, DYBTAA060, DYBUAA017, DYBUAA034, DYBUAA051, and DYBUAA068,

Why it was recalled

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

Root cause (FDA determination)

Other

Action the firm took

On Nov 10, 2017 Bard Medical sent notification letter to all their consignees informing them of the following: Action required: "Immediately examine your inventory and quarantine product subject to this recall. Please refer to CritiCore MonitorAffected Serial Numbers (Attachment 2) to help you locate the affected product serial number. Do not use or furtherdistribute any affected product. "Please complete and return the accompanying Recall & Effectiveness Check Form (Attachment 1) attached to thisletter regardless of whether you have any of the affected product. Additional instructions for product return arecontained on the form. "If you have further distributed any units with the referenced serial numbers, please identify your customers and notifythem at once of this product recall: Your notification should include a copy of this letter and the accompanying enclosures. Please complete this form by 11/24/2017 and fax to 1-770-784-6469 or email a scanned copy to BMD.FieldAction@crbard.com . If you have affected product, please contact the BMD Customer Service via phone at 1-800-526-4455 option 5 and again option 5 or email BMD.FieldAction@crbard.com to obtain a Return Goods Authorization number (RGA #). Fax this form to 1-770-784-6469 or email a scanned copy to BMD.FieldAction@crbard.com. Attn: Recall Coordinator This recall should be carried out to the user level.

Recalling firm

Firm: C.R. Bard, Inc.
Address: 8195 Industrial Blvd NE, Covington, Georgia 30014-1497

Distribution

Distribution pattern: 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

Timeline

Recall initiated: 2017-11-10
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #164531. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.